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<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
Direct the development and establishment of processes in Process Development. This individual is accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up. The individual will provide technical expertise and leadership in science &amp; technology and requires close collaboration with internal stakeholders.
JOB RESPONSIBILITIES
<ul>
<li>Accountable for supporting the establishment of downstream vector platform from small scale through intermediate scale (50L) for adeno-associated virus, lentiviral and retroviral vector processes.</li>
<li>Monitoring and reporting on process performance, identifying opportunities, and implementing changes to improve process, product safety, and product quality.</li>
<li>Support process optimization efforts leading to increases in process robustness, cost reduction and improvements in viral yield and purity.</li>
<li>Design and execute experiments independently: accurately record, analyze, and communicate data to senior management and team members.</li>
<li>Frequently communicate with external clients to design experiments and report out on generated data</li>
<li>Maintain open communication via one-on-one and team meetings.</li>
<li>Stay current with relevant technologies and client/industry including identifying new approaches.</li>
<li>Perform and lead single-use system design manifold, selection, implementation, configurations in between Upstream bioreactor and downstream unit operations and control strategies.</li>
<li>Develop appropriate and detailed SOP and BPR for downstream processes including equipment and system use</li>
<li>Responsible for the process transfer from/to clients and to in-house manufacturing team(s).</li>
<li>Maintain external technical relationships and collaborate with equipment and material suppliers.</li>
<li>Serve as process SME for client-facing and internal programs.</li>
<li>Ensure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the assigned functional area.</li>
</ul>
SPECIAL JOB REQUIREMENTS
<ul>
<li>Adaptability required as work schedule may change based on business needs</li>
<li>Criminal background check required</li>
<li>Other duties as assigned</li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
BS or MS in biological engineering
Desired
ON-THE-JOB EXPERIENCE
 
2-8+ years of relevant industry experience
Essential
Solid foundation in the fundamentals of biochemical engineering, virology and cell biology
Essential
Experience with industry standard chromatography and filtration methods
Essential
Ability to hypothesize and drive key experiments for internal and external programs
Essential
Entrepreneurial experience dealing with customers in product development
Desired
Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing Organizations
Desired
Experience with cell culture technologies, molecular biology, upstream processing, and aseptic processing
Desired
Understanding of analytical assays used in the characterization of biologics
Desired
SKILLS / ABILITIES
 
Working knowledge of AKTAs and UNICORN software
Essential
Familiar with tangential flow filtration skids
Desired
Ability to interface successfully with multi-disciplined teams. 
Desired
Extremely detail-oriented with strong technical skills &amp; mechanically inclined/knowledge of hand tools
Desired
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
<ul>
<li>Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning.</li>
<li>Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities.</li>
<li>Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock.</li>
<li>Occasionally exposed to extremely loud noise levels</li>
<li>Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required.</li>
</ul>
Movement
<ul>
<li>Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms.</li>
<li>Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl.</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 25 pounds.</li>
<li>Occasionally lift and/or move up to 50 pounds.</li>
</ul>
Vision 
<ul>
<li>Frequently utilize close vision and the ability to adjust focus</li>
</ul>
Communication
<ul>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
Pay Range: The annual salary range for this position is $100,000-$130,000.
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
Solutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

Scientist II/III, Downstream Process Development

<h3>Job Description</h3>
Shift:
Monday through Friday, 8:00 AM - 5:00 PM

Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.

SUMMARY
Responsible for providing or overseeing the analysis, administration and oversight of standard chemistry/biochemistry policies, programs and practices; feedback and guidance regarding the analysis of samples using fundamental professional and technical knowledge of chemistry/biochemistry or related instrumentation, wet chemistry testing,&nbsp;and procedures.

NOTE: This is an Evergreen role where we are collecting resumes for future openings

Compensation: $28.00 per hour

ESSENTIAL FUNCTIONS
<ul>
<li>
Provides fundamental analysis in support of standard testing materials, products and/or devices utilizing standard analytical instrumentation; follows Standard Operating Procedures and methods to perform testing.
</li>
<li>
Provides fundamental review, analysis, interpretation, and documentation of testing results.
</li>
<li>
Overseeing or reviewing, completing, and processing various types of standard chemistry/biochemistry forms, documents, databases, and related materials and information.
</li>
<li>
Provides fundamental analysis and interpretation and counsel to staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves standard operations.
</li>
<li>
Provides standard research, feedback, and decisions to resolve management and employee questions and requirements; assists with receiving customer feedback and coordinating resources and responses as required.
</li>
<li>
Analyzes and reviews process, results, feedback, and related chemistry/biochemistry information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management.
</li>
<li>
Ensures the accuracy of more fundamental tests, equipment, actions, procedures and operational databases, reports, and related details through audits, queries, and operational reviews; works with teams to resolve discrepancies; resolves discrepancies or escalates discrepancies to ensure quality assurance in testing process/results.
</li>
<li>
Assists with developing or participating in chemistry/biochemistry or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management.
</li>
<li>
Cleans, maintains, prepares, and calibrates equipment, samples, and related areas.
</li>
<li>
Interprets and applies department policies and procedures and assists with applicable laws, rules, and regulations; receives guidance within these areas as needed.
</li>
<li>
Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team.
</li>
<li>
Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment.
</li>
</ul>
QUALIFICATIONS
Education and Experience
Bachelor's degree in chemistry/biochemistry, or a closely related field; OR an equivalent combination of education, training, and experience.
Required Knowledge and Skills
Required Knowledge
<ul>
<li>
Fundamental principles, practices, and techniques of chemistry/biochemistry.
</li>
<li>
Standard understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures.
</li>
<li>
Fundamental methods to resolve chemistry/biochemistry problems, questions, and concerns.
</li>
<li>
Standard understanding of applicable chemistry/biochemistry laws, codes, and regulations.
</li>
<li>
Understanding of standard testing tools, instruments, and calibration.
</li>
<li>
Computer applications and systems related to the work.
</li>
<li>
Principles and practices to serving as an effective project team member.
</li>
<li>
Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations.
</li>
<li>
Correct business English, including spelling, grammar, and punctuation.
</li>
</ul>
Required Skills
<ul>
<li>
Performing fundamental professional-level chemistry/biochemistry duties in a variety of assigned areas.
</li>
<li>
Overseeing and administering standard chemistry/biochemistry functions.
</li>
<li>
Training others in policies and procedures related to the work.
</li>
<li>
Serving as a team member and the development and management of projects.
</li>
<li>
Operating in a both a team and individual contributor environment.
</li>
<li>
Interpreting, applying, and explaining applicable laws, codes, and regulations.
</li>
<li>
Preparing fundamental functionals reports, correspondence, and other written materials.
</li>
<li>
Using initiative and independent judgment within established department guidelines.
</li>
<li>
Using tact, discretion, and prudence in working with those contacted in the course of the work.
</li>
<li>
Performing effective oral presentations to large and small groups across functional peers and the department.
</li>
<li>
Contributing effectively to the accomplishment of team or work unit goals, objectives and activities.
</li>
<li>
Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work.
</li>
</ul>

Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.

Benefits When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.

Equal Opportunity Employer
Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Associate Scientist I

<h3>Job Description</h3>
Job DescriptionDescription:
We are Pest-End - one of the fastest-growing, family-owned, and operated wildlife and pest management companies in New England. Our company culture is single-handedly the most essential component of our continued success. We believe that to succeed as a business, our team members must thrive as individuals. That encompasses passionate and empathetic leadership, a 'think big, act small' mentality, and providing career paths that promote growth and internal promotions. We provide you with everything needed to be successful, competent, and confident in your role with Pest-End.
Who we need
Our business and team are growing. We are currently hiring wildlife service technicians in Massachusetts, looking to begin or continue a career in professional wildlife control. Qualified candidates will have skills or experience with carpentry work.
Wildlife technicians thrive on independence and enjoy occasional detective work to solve every day to intricate wildlife problems for our residential and business customers. Due to the nature of our work, candidates must be willing to work both outdoors and indoors throughout the year. Some scenarios require our service technicians to use ladders to more efficiently and effectively complete a job. Pest-End provides ladder safety training for our team.
Job Responsibilities:
<ul>
<li>Driving company vehicle to customer locations.</li>
<li>Meeting with customers to diagnose and explain services needed.</li>
<li>Inspecting interior and exterior of customers' properties. This position requires the use of a ladders and climbing on roofs, or entering tight places like a crawl space.</li>
<li>Capturing nuisance wildlife in a safe manner.</li>
<li>Performing basic exclusion and repair work on the areas where wildlife enter the customers' home or business.</li>
<li>Obtaining state wildlife certification</li>
<li>Obtaining state pesticide licenses to assist our Intergrated Pest Management team.</li>
<li>Maintain notes and records about customers and the services they have had.</li>
<li>Keeping an open line of communication between yourself, office staff, and managers.</li>
<li>Ability to lift 40 lbs + comfortably.</li>
</ul>
What our benefits and perks look like:
<ul>
<li>Paid time off and holidays</li>
<li>401K with an employer match up to 3%</li>
<li>Monthly cell phone stipend</li>
<li>Comprehensive health, dental, and vision insurance</li>
<li>Employer funded life insurance policy</li>
<li>Paid training, and state certifications provided for non-licensed new hires</li>
<li>Company vehicle and gas card</li>
<li>Short and long term disability through Aflac</li>
<li>Company supplied uniforms</li>
</ul>
 
Requirements:
What we require:
<ul>
<li>Valid driver's license with a driving record free of major incidents</li>
<li>18 years or older</li>
<li>2+ years of carpentry experience </li>
<li>Complete a pre-employment background check and drug screening</li>
<li>High school diploma or equivalent</li>
<li>Ability to work full-time with the potential for overtime during May - September</li>
</ul>
Physical Requirements:
While performing the duties of this job, the team member is frequently required to stand, walk, sit, climb, bend, kneel and crawl within tight spaces. Specific hearing and vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The employee may occasionally lift and/ or move up to 50 pounds. Additionally, wildlife technicians should be comfortable with ladder work and on roofs and be able to lift and maneuver up to a 40-foot ladder. 
 
Pest-End, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Wildlife Service Technician

<h3>Job Description</h3>
Job Description Can You See What Others Miss?
If you instinctively catch the thousandth others overlook, let’s talk. Senior Metal Bellows designs and builds custom-engineered metal bellows that power missions in aerospace, medical, defense, and energy. We need a CMM Metrology Specialist who thrives on accuracy, collaboration, and continuous improvement.
 What Will You Do?
<ul>
<li>Turn complex engineering drawings into actionable inspection plans</li>
<li>Set up and perform complex precision inspections using advanced tooling</li>
<li>Apply GD&amp;T (ANSI Y14.5) to validate dimensional and geometric requirements</li>
<li>Partner with engineering to develop new inspection techniques and improve existing ones</li>
<li>Conduct first piece checks and complete AS9102 first article inspections</li>
<li>Dig into nonconforming trends, support root-cause analysis, and recommend process improvements</li>
<li>Operate CMMs, optical comparators, micrometers, verniers, drop indicators, height gages, and more</li>
</ul>
 What Do You Bring?
<ul>
<li>Expert-level understanding of precision inspection and geometric dimensioning</li>
<li>Hands-on CMM experience and strong skills with manual metrology tools</li>
<li>Ability to interpret intricate drawings with exceptional attention to detail</li>
<li>Team-first communicator who collaborates well across functions</li>
<li>Problem-solver driven to refine processes continuously</li>
</ul>
 Why Join Us?
<ul>
<li>70+ years of innovation with parts that must perform when failure isn’t an option</li>
<li>Culture built on collaboration, respect, trust, and excellence</li>
<li>Global opportunities as part of Senior plc across 12 countries</li>
<li>Convenient Sharon, MA location just off Route 95</li>
</ul>
 Pay Transparency
Hourly Rate Range: $29.00 - $34.00. Final rate will be determined by relevant experience, skills, and qualifications.
 Ready to Build What’s Next?
Apply now—bring your metrology expertise to a team that values craftsmanship and precision.
 Legal &amp; Compliance
All your information will be kept confidential according to EEO guidelines.
Access to our facility (and, therefore, employment) is restricted under the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR) to U.S. Citizens, lawful permanent residents of the United States and properly-licensed foreign persons.

CMM Metrology Specialist

<h3>Job Description</h3>
Job DescriptionSalary: $50,000 - $70,000 
JOB SUMMARY
The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Collects Environmental Monitoring Samples at client manufacturing sites on a daily basis in the greater Boston area.</li>
<li>Sample collection types include: air viable, surface viable, water and compressed gas samples. Samples are then subsequently submitted to the lab for analysis.</li>
<li>Understands the importance of aseptic technique and the critical role it plays in EM sample collection.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.</li>
<li>Performs routine data generation and problem solving with a minimal rework.</li>
<li>Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
</ul>
 
SHIFT
Wednesday - Saturday 1st Shift
 
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.

Microbiologist I, EM

<h3>Job Description</h3>
Job Description
Role Description
We are seeking a motivated and detail-oriented Chemist to join our team in Londonderry, NH. This full-time, on-site role is ideal for someone passionate about laboratory work, quality control, and innovative product development. You will play a key role in ensuring product integrity through rigorous testing and contribute to the creation of new formulations through research and development.
Key Responsibilities:
<ul>
<li>Conduct quality control testing on raw materials and finished products.</li>
<li>Utilize analytical techniques and laboratory equipment to ensure product consistency and compliance.</li>
<li>Support research and development efforts for new product formulations.</li>
<li>Maintain accurate documentation of test results and formulation data.</li>
<li>Collaborate with cross-functional teams to improve processes and product performance.</li>
<li>Apply polymer chemistry knowledge to enhance product innovation (preferred).</li>
</ul>
Qualifications:
<ul>
<li>Bachelors or Associate degree in Chemistry or a related field.</li>
<li>Strong laboratory skills and hands-on experience with analytical instruments.</li>
<li>Proven experience in quality control and R&amp;D environments.</li>
<li>Ability to work independently and collaboratively in a team setting.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Experience with polymer chemistry is a plus.</li>
</ul>
<ul>
<li></li>
</ul>

Chemist

<h3>Job Description</h3>
Job DescriptionRole Summary
<ul>
<li>Responsibilities: You will be responsible for leading a range of projects that involve devising and performing statistical analysis plans and then communicating the methodologies and results of these to our clients in the healthcare sector</li>
<li>Salary: $100,000 per annum</li>
<li>Benefits: Hybrid working options, generous holiday allowance, flexible working hours, private medical and dental insurance, 401K plan, life insurance, full funding for external training, comprehensive travel insurance and more</li>
<li>Role Type: Full-time, permanent </li>
<li>Start Date: We are currently recruiting for start dates throughout 2026 and you will be asked to state your preference on your application form</li>
<li>Location: This role is available in our Boston office </li>
</ul>
About the Role
Our Statistics team provide statistical and analytical expertise across Costello Medical, devising statistical analysis plans and performing data analysis within R, Excel, Stan, SQL and BUGS software. They are also responsible for communicating the methodologies and results in both written and oral formats to drug and device manufacturers, and doctors. The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic statistical analysis of individual patient data, regression analysis, survival analysis and complex Bayesian network meta-analysis using both standard and emerging methods.
The Senior Statistician will lead statistics projects, working very closely with the Consultant or Team Lead as well as colleagues from all specialities, to ensure that statistics projects are delivered to an exceptionally high standard, on time and in line with client expectations. This involves providing strategic advice to clients at project initiation, supervising the project team and regular interaction with external stakeholders by teleconference, email and in person. The Senior Statistician will also be central to the quality control of the project, involving the review of colleagues' work and the provision of constructive feedback.
Our team typically work on several projects at one time and the results of each analysis can feed into publications, value materials, health economic models or health technology assessment submissions. You will therefore be exposed to a wide variety of our service and a broad range of therapeutic areas. To read more about our recent articles and publications, please visit our website: <a href="https://www.costellomedical.com/research/articles-publications/" target="_blank">https://www.costellomedical.com/research/articles-publications/</a>
You will also play a key role in contributing to business development by developing and maintaining excellent client relationships and identifying opportunities to provide additional services to clients within projects. There may also be opportunities to line manage and mentor our Statistician Interns.
Career Progression
Senior Statisticians are supported to progress to the Consultant Statistician role. Consultant Statisticians manage a range of projects and have full responsibility for client communication on projects, as well as leading budgeting plans and business development efforts. In addition to technical project delivery, Consultant Statisticians line manage team members and have internal responsibilities spanning areas such as recruitment and training.
To learn more about the personal and professional development opportunities at Costello Medical, explore first-hand career profiles from our colleagues about their experiences with the company: <a href="https://www.costellomedical.co.uk/careers/working-at-costello-medical/" target="_blank">https://www.costellomedical.co.uk/careers/working-at-costello-medical/</a>
About Costello Medical
Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access, and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies, and charitable organisations. We have been listed in the Top 100 Best Companies to Work For list since 2017 and were proud to receive B Corporation accreditation in 2022. Learn more about us, our work, and our mission on our website: <a href="https://www.costellomedical.com/" target="_blank">https://www.costellomedical.com/</a>
Requirements
About You
We are looking for individuals who are collaborative, self-motivated and enthusiastic, with a strong and demonstrable background in the HEOR sector. You will take pride in producing exceptionally high-quality work and will relish the opportunity to build successful client relationships. You will identify and capitalise on opportunities to go above and beyond for clients and exceed their expectations wherever possible. You will be someone who has a genuine desire to play an active role in the development of our growing team. You will enjoy using your experience to train and mentor others and will be skilled at delivering effective feedback to support your colleague’s professional development. 
You will thrive in a fast-paced environment, be highly organised and able to manage timelines across multiple projects. Additionally, you will be willing to step up and support your project team as needed.
This role is suited to those who have professional experience, of typically no less than 2 years, in applying economic and mathematical modelling techniques within an industry setting, ideally within a pharmaceutical, medical devices or consulting company. Specifically, we are looking for candidates with experience: 
<ul>
<li>Working directly with clients from project initiation to completion</li>
<li>Leading a project team, including delegating tasks and managing the time of others coupled with the ability to manage timelines across multiple projects at once and the flexibility to respond to changing deadlines</li>
<li>Communicating directly with clients including responding to different communication styles, as well as a proven ability to build robust and sustainable client relationships</li>
</ul>
In addition, essential requirements for the role are:
<ul>
<li>A degree level or higher qualification in a scientific or mathematical discipline (minimum GPA 3.3) is required. A focus on statistics and data analysis is essential</li>
<li> The technical and mathematical ability, coupled with exceptional written and oral communication skills, to explain complex techniques and results to non-experts, and to teach and mentor others in the Statistics team</li>
<li>An excellent understanding of and extensive experience in the R programming language, and the willingness and ability to rapidly develop your programming skills</li>
<li>A willingness to trial, explore or recommend new software or techniques that may suit specific projects</li>
<li>Exceptional attention to detail and a high degree of accuracy in technical and written work, along with the ability to maintain exceptional customer service and the quality of deliverables under multiple competing demands</li>
<li>The ability to use your initiative and work independently, in addition to working collaboratively within project teams</li>
<li>Excellent written English is fundamental; this will be assessed during the selection process</li>
</ul>
Desired requirements for the role are: 
<ul>
<li>A Masters degree or PhD in a scientific or mathematical discipline</li>
<li>Experience with Stan, Python, SQL, or other programming languages used for data analysis</li>
<li>Awareness of data standards for clinical research and statistical analysis (e.g. CDISC, SDTM, ADaM, ICH Statistical Principles for Clinical Trials)</li>
</ul>
Benefits
What We Offer
<ul>
<li>A starting salary of $100,000 per annum</li>
<li>A discretionary profit share bonus paid twice per year</li>
<li>Private medical insurance with a company contribution </li>
<li>Dental and vision cover </li>
<li>23 days’ vacation leave increasing by 1 day to a maximum of 27 days. 6 public holidays plus 1 floating holiday </li>
<li>The chance to work from home for up to half of your working time</li>
<li>Retirement savings via a 401k plan</li>
<li>Paid funding for external education and study leave</li>
<li>Life insurance </li>
<li>Comprehensive travel insurance</li>
<li>Flexible and reasonable working hours</li>
<li>Regular company-funded social activities </li>
</ul>
Please click here to learn about our reward package and the other benefits of working for Costello Medical: <a href="https://www.costellomedical.com/careers/benefits-package-in-the-us/" target="_blank">https://www.costellomedical.com/careers/benefits-package-in-the-us/</a>
The Application Process
You are required to submit your resume and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your resume should clearly state the dates of all qualifications and grades achieved where applicable.
Then, our recruitment process includes a telephone interview with a member of the Talent Acquisition team, followed by an assessment for you to complete in your own time. If successful, you will be invited to an interview which will include a short presentation you can prepare for in advance. Our standard recruitment process lasts around 1 month, however, this can be adapted if necessary. 
As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide: <a href="https://www.costellomedical.com/reasonable-adjustments/" target="_blank">https://www.costellomedical.com/reasonable-adjustments/</a>
Please note that, whilst we embrace AI to innovate and improve processes, your role may involve confidential data that cannot be uploaded to AI. Therefore, it is important for us to assess your own skills and abilities, so we recommend that you do not rely solely on this technology to generate any application materials.
Visa Sponsorship
We welcome applications from international candidates, but we are unfortunately unable to provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we are able to consider those on a temporary visa, such as an OPT visa.

Senior Statistician

<h3>Job Description</h3>
Job Description
About This Role:
The Principal Statistician will provide technical and statistical leadership that empowers teams within Endoscopy and across the company's global network to deliver breakthrough solutions. The Principal Statistician's expertise will be instrumental in driving new product development from concept to launch, ensuring that every decision is grounded in robust data and statistical insight.
 
This role will be a key mentor and trusted advisor, not only for the R&amp;D organization but also for cross-functional teams worldwide. By fostering a culture of learning and continuous improvement, this position will elevate the statistical &amp; problem-solving acumen of engineers, scientists, and technical professionals, helping them translate complex data into actionable strategies that accelerate product development.
 
The work will directly contribute to launching innovative products that advance patient care. The Principal Statistician will guide teams through the rigorous application of statistical methods that will help ensure that the products meet the highest standards of quality and safety to make a tangible difference in the lives of patients around the world.
 
Responsibilities will include:
<ul>
<li>Provide statistical expertise and support to R&amp;D using statistical methods associated with product and process development, design assurance, and problem-solving in root cause investigations.</li>
<li>Interpret data and provide insight into the underlying factors driving the results to advise engineers on the best strategies to move forward, not just on the data analysis</li>
<li>Apply a variety of statistical analyses and techniques to data generated by R&amp;D, Process Development, and other technical groups.</li>
<li>Create and maintain statistics-related procedures and tools for the company site and the global network.</li>
<li>Collaborate with Global Statisticians and cross-functional teams working towards continual improvement of the application and use of statistics across various projects and business initiatives.</li>
<li>Identify and lead projects that improve efficiencies in product and process development through designed experiments, reduced sampling methodologies, and advanced or automated data analysis.</li>
<li>Provide feedback to cross-functional development teams during design reviews on the application and insights from statistical analysis tools.</li>
<li>Develop and deliver training (classroom and virtual options) on the appropriate use of statistical methods with R&amp;D, Process Development, and other technical groups.</li>
<li>Perform ad hoc statistical analyses and provide guidance as required.</li>
<li>Demonstrate a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures.</li>
</ul>
 
Required qualifications:
<ul>
<li>Bachelor's degree in Mathematics, Statistics, Physics, or Engineering</li>
<li>8+ years of experience in an industry role, preferably within medical devices; experience in a regulated environment is required</li>
<li>5+ years of experience using Minitab, Design Expert, or other relevant statistical software</li>
<li>Proven ability to apply statistical analysis in a professional setting; highly self-motivated and results-driven </li>
</ul>
 
Preferred qualifications:
<ul>
<li>Master's or PhD in Mathematics, Statistics, Engineering, or a related field</li>
<li>Experience working in or closely with R&amp;D or Development Engineering teams</li>
<li>Demonstrated application of statistical tools to support project deliverables (e.g., test method validation, design verification testing)</li>
<li>Six Sigma Black Belt or Master Black Belt certification</li>
</ul>

Principal Statistician

<h3>Job Description</h3>
Job Description
Come join CCRM Fertility, a global pioneer in fertility treatment, research, science, specializing in IVF, fertility testing, egg freezing, preimplantation genetic testing, third party reproduction and egg donation. As a member of CCRM Fertility’s diverse team of professionals, you will be a part of helping families grow and changing lives. We take pride in providing our employees with meaningful employment, a supportive culture, and a well-balanced personal &amp; work life alignment. For more information, visit <a href="http://www.ccrmivf.com" target="_blank">www.ccrmivf.com</a>
Location Address: 
Department: IVF Laboratory
Work Schedule: Monday – Friday (8:00am – 4:30pm)
What We Offer Our Team Members:
<ul>
<li>Generous Paid time-off (PTO) and paid holidays</li>
<li>Medical, Dental, and Vision Insurance</li>
<li>Health benefits eligible the first day of the month following your start date.</li>
<li>401(k) Plan with Company Match (first of the month following 2 months of service)</li>
<li>Basic &amp; Supplement Life Insurance</li>
<li>Employee Assistance Program (EAP)</li>
<li>Short-Term Disability</li>
<li>Flexible spending including Dependent Care and Commuter benefits.</li>
<li>Health Savings Account</li>
<li>CCRM Paid Family Medical Leave (eligible after 1 year)</li>
<li>Supplemental Options (Critical Illness, Hospital Indemnity, Accident)</li>
<li>Professional Development, Job Training, and Cross Training Opportunities </li>
<li>Bonus Potential</li>
</ul>
What You Will Do: The Senior Embryologist will be responsible for performing all procedures in the IVF Laboratory under the direction of the IVF Laboratory Supervisor. The Senior Embryologist must demonstrate knowledge and skills related to the various procedures performed in the IVF Laboratory. The Senior Embryologist reports directly to the IVF Lab Supervisor.
<ul>
<li>Perform daily, weekly, and periodic function checks and maintenance on equipment and trouble shoot equipment problems and make appropriate decisions for repair, with guidance.</li>
<li>Follow appropriate blood borne pathogen handling and disposal procedures.</li>
<li>Perform all aspects of media/medium preparation with sterile technique for each case and documents the lots used.</li>
<li>Process semen for IVF procedures according to IVF lab protocol.</li>
<li>Assist physician during egg retrievals and is able to locate and assess all oocytes retrieved in a timely manner. Able to trim oocytes without trauma or injury to the oocytes.</li>
<li>Adhere to the IVF lab’s double signature and check system when performing procedures to ensure correct identity of eggs, sperm, and embryos.</li>
<li>Document all patients’ results into the IVF Lab information system (LIS).</li>
<li>Perform daily fertilization checks which includes “cleaning” embryos with minimal trauma (insemination cases) to observe fertilization.</li>
<li>Assess fertilization by observation of pronuclei and polar bodies.</li>
<li>Perform freezing and thawing of human embryos according to IVF lab protocol with a high survival rate.</li>
<li>Perform oocyte inseminations according to IVF lab protocol.</li>
<li>Able to hyal and strip oocytes for ICSI with minimal trauma.</li>
<li>Perform Intracytoplasmic Sperm Injection (ICSI) according to IVF lab procedures resulting in high fertilization rates.</li>
<li>Assist physician with embryo transfer and ensures proper identification of the patient with a “time-out” before the transfer.</li>
<li>Assist physician during PESA, MESA and TESE procedures by locating and processing sperm found according to IVF lab procedures.</li>
</ul>
<ul>
<li>Perform biopsy procedures, including trophectoderm biopsy, resulting in high number of embryos returning a test result. Embryos biopsied result in a high survival rate when thawed and an acceptable implantation rate when transferred.</li>
<li>Other duties as assigned.</li>
</ul>
What You Bring:
<ul>
<li>Bachelor’s Degree in Biology, Chemistry, or Microbiology required.</li>
<li>Medical technology licensure/certificate required if Embryologist completed a medical technology university-based program.</li>
<li>5+ years’ experience in laboratory or scientific research required (Med laboratory preferred).</li>
<li>Computer and database experience preferred.</li>
</ul>
Working Conditions: The physical demands described here are representative of those which should be met, with or without reasonable accommodation (IAW ADA Guidelines), by an employee to successfully perform the essential functions of this job. This job operates in a professional office and clinical setting. This role routinely uses standard office equipment such as computers, including computer keyboards and mice; telephones; photocopiers; scanners; filing cabinets. While performing the duties of this job, the employee is regularly required to communicate with others. The employee is frequently required to sit; will occasionally stand and/or walk; use hands and fingers to grasp, pick, pinch, type; and reach with hands and arms. Employees should have the visual acuity to perform an activity such as: preparing and analyzing data and figures, viewing a computer terminal, extensive reading, and operation of standard office machines and equipment. 
CCRM’s Compensation: The salary range represents the national average compensation for this position. The base salary offered will vary based on location, experience, skills, and knowledge. The pay range does not reflect the total compensation package. Our rewards may include an annual bonus, flexible work arrangements, and many other region-specific benefits.
Pre-Employment Requirements: All offers of employment are conditional upon the successful completion of the CCRM Fertility onboarding process, including verification of eligibility and authorization to work in the United States. This employer participates in the E-Verify Program in order to verify the identity and work authorization of all newly hired employees.
Equal Employment/Anti-Discrimination: We are an equal-opportunity employer. In all aspects of employment, including the decision to hire, promote, discipline, or discharge, the choice will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Senior Embryologist

<h3>Job Description</h3>
The Center for Engineering in Medicine &amp; Surgery (CEMS) is a place where scientific rigor and creativity are matched by a sense of sharing and community, bringing technology to the forefront of biomedical research and the practice of medicine. The CEMS draws strength from its diversity and collaborative spirit, and from its affiliations with surrounding biomedical research institutions including the Massachusetts General Hospital, the Harvard Medical School, the Shriners Burns Hospital, and the Massachusetts Institute of Technology. Interactions both within and outside the CEMS provide excellent opportunities for training and next career steps. The emphasis of CEMS on collaboration serves to remove the boundaries separating the engineering, scientific and clinical disciplines. The physical layout and research activities in the CEMS follow the same principles with an open-bay configuration, interdisciplinary group meetings and a focus on highly challenging cutting-edge problems.
 
We have an opening for a junior technical staff role (Bachelors level training in relevant fields with &lt;1 years experience). Relevant experience in small animal surgery, molecular biology, mammalian cell culture including hepatocytes and endothelial cells are preferred. All our technical staff work together with PhD students, postdoctoral fellows and faculty and participate in research, and therefore good analytical skills and independent thinking are critical. Excellent communication and organizational skills are a must in our fast paced environment featuring translational research ranging from cells to organ transplantation and clinical studies.
 
Over the last decade all staff with similar roles have been acknowledged as authors in scientific publications due to their intellectual contributions. The vast majority have moved on to receive graduate training in MD, PhD or MBA programs, including many ivy league schools. The others have found high-paying industry positions. We are looking forward to see our new colleagues meet and exceed these high standards of success.
 
Application package&nbsp;(IMPORTANT)
Please include in your application i) a brief cover letter, including a listing laboratory skills and other scientific methods mastered, and ii) a list of 2 references willing to submit reference letters at a later date. Applications can be done either directly via linkedin, or if preferred, by sending an email to <a href="mailto:kuygun@mgh.harvard.edu" target="_blank">kuygun@mgh.harvard.edu</a> with a pdf attachment for the above items required.

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