Waregem, Flanders, Belgium · Hybrid
$125k–$209k/yr
Position Summary You will manage the Manufacturing Science and Technology (MSAT) Drug Product technical delivery for drug product manufacturing of a defined product or product family with a primary focus on New Product I…
Skills: Technology Transfer, Process Validation, Drug Product Manufacturing, GMP, Risk Assessment
Springfield, Massachusetts, United States · On-site
$34/hr–$58/hr
Respiratory Therapist Location: Pulmonary Function Lab Schedule: Part time, 32 hours Summary Respiratory Therapists, working under the general supervision of a physician, are responsible for evaluating, diagnosing, and t…
Skills: Pulmonary Function Testing, Interventional Diagnostics, Blood Gas Analysis, Medical Gas Therapy, Aerosol Therapy
Cambridge, Massachusetts, United States · Hybrid
$149k–$215k/yr
Job title: Senior Principal Scientist Location: Cambridge, MA About the Job We are seeking a highly motivated Senior Principal Scientist to spearhead the execution and expansion of our mast cell disorders Research & Deve…
Skills: Hematopoietic Stem Cell Biology, Mast Cell Disorders, Rare Disease Research, Target Identification, Preclinical Strategy
Framingham, Massachusetts, United States · Hybrid
$90k–$130k/yr
Job title: Senior Manager Quality, EM&S Gen Med North America Location: Framingham, MA About the Job This role reports to the Senior Director, Quality, EM&S Gen Med NA and is part of a team that has primary responsibilit…
Skills: cGMP Compliance, Quality Management System, Quality Assurance, Regulatory Compliance, Contract Manufacturing Oversight
Weston, Massachusetts, United States · On-site
Job DetailsJob Location: Regis College Campus - Weston, MA 02493Position Type: AdjunctSummary Regis College is seeking an adjunct faculty member to teach DH 106 Head/Neck Anatomy & Embryology (Mondays 8-10:50am) during t…
Skills: Teaching, Curriculum Preparation, Academic Assessment, Student Engagement, Dental Hygiene Instruction
Weymouth, Massachusetts, United States · On-site
$32/hr–$60/hr
Job Summary: In keeping with Shields Health Care commitment to excellence, the PET technologist will provide a professional, caring atmosphere to all customer groups, while maintaining a fast-paced, multi-tasked oriented…
Skills: PET Imaging, Nuclear Medicine, IV Insertion, Patient Positioning, Hot Lab Management
Woburn, Massachusetts, United States · On-site
Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend o…
Skills: HR Operations, Employee Relations, Total Rewards, Collaboration, HR Administration
Massachusetts, United States · On-site
At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons…
Skills: Intraoperative Neuromonitoring, Patient Care, Medical History Collection, Waveform Analysis, Technical Troubleshooting
Weymouth, Massachusetts, United States · On-site
$40/hr–$60/hr
Job Summary: Shields Health Care Group’s MRI Technologists support the integrity of the organization with their commitment to excellence. The MRI technologist will provide a professional, caring atmosphere to all custome…
Skills: MRI Scanning, Patient Positioning, Contrast Administration, Patient Safety, Interpersonal Skills
Tewksbury, Massachusetts, United States · On-site
$57k–$109k/yr
Date Posted: 2026-07-08 Country: United States of America Location: US-MA-TEWKSBURY-TB1 ~ 50 Apple Hill Dr ~ ASSABET BLDG Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active a…
Skills: RF/Microwave System Design, Phased Array Antennas, Electromagnetic Simulation, HFSS, ADS
Dracut, Massachusetts, United States · On-site
$18/hr–$18/hr
Job Summary -The Cultivation Technician is responsible for assisting cultivation management in the day-to-day functions of the cultivation production areas, including propagation, cultivation, cure, and harvest. The Cult…
Skills: Plant Care, Pruning, Harvesting, Trimming, Quality Control
Framingham, Massachusetts, United States · On-site
$138k–$190k/yr
At Bose Corporation, we believe sound is the most powerful force on earth — and for over 60 years, we have been a company built on innovation, excellence, and independence. Privately owned, fiercely customer-focused, and…
Skills: Digital Signal Processing, Audio Processing, Speech Processing, C, Python
Acton, Massachusetts, United States · On-site
$77k–$116k/yr
Job Summary The NPI and Validation Engineer plays a key role in bringing new medical device products from development into manufacturing while ensuring processes are efficient, compliant, and high quality. This position …
Skills: NPI, Process Validation, Design Transfer, Design For Manufacturability, Data Analysis
Boston, Massachusetts, United States · On-site
$18/hr–$26/hr
Site: The General Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As …
Skills: Specimen Processing, Laboratory Information System, Inventory Management, Specimen Handling, Safety Compliance
Westford, Massachusetts, United States · On-site
$99k–$199k/yr
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnost…
Skills: Machine Learning, Deep Learning, Computer Vision, Python, PyTorch
Foxborough, Massachusetts, United States · On-site
$127k/yr
Site: The Brigham and Women's Hospital, Inc. Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our missio…
Skills: IV Admixtures, Drug Information, Ambulatory Care, Drug Distribution, Medication Management
Holyoke, Massachusetts, United States · On-site
$19/hr–$23/hr
Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for pe…
Skills: Supervision, Specimen Processing, Quality Assurance, Data Entry, Microsoft Office
Waltham, Massachusetts, United States · Remote OK
$136k–$167k/yr
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need fo…
Skills: Benefit Investigations, Prior Authorization, Case Management, Reimbursement Processes, Payer Policy Expertise
Cambridge, Massachusetts, United States · Hybrid
$184k–$253k/yr
About This Role: As the Director of Procurement - Global Development & Medical Services, you will play a pivotal role within the Research, Development, and Medical Services Procurement team. This position is integral to …
Skills: Category Strategy Leadership, Supplier Relationship Management, Spend Analytics, Cross Functional Leadership, Negotiation Leadership
Webster, Massachusetts, United States · On-site
$128k–$161k/yr
Are you a current UMass Memorial Health caregiver? Apply now through Workday. Hiring Range: $127,587.20 - $160,763.20 Please note that the final offer may vary within this range based on a candidate’s experience, skills,…
Skills: Psychiatric Nursing, Mental Health Evaluations, Patient Care Case Presentation, Clinical Practice, Interdisciplinary Collaboration
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Manage MSAT Drug Product technical delivery with a focus on New Product Introduction and successful product launches. Lead technology transfers, maintain product control strategies, and manage complex technical investigations and regulatory submissions.
Requires a Bachelor's degree in a scientific or engineering discipline and at least 8 years of experience in pharmaceutical development or MSAT. Must have hands-on experience with oral solid dose manufacturing and a strong knowledge of GMP and regulatory expectations.
Position Summary
You will manage the Manufacturing Science and Technology (MSAT) Drug Product technical delivery for drug product manufacturing of a defined product or product family with a primary focus on New Product Introduction (NPI) and successful product launches, including delivering successful right-first-time product qualifications. You will work with cross-functional teams across functions to ensure robust product control strategies are implemented at manufacturing sites. We value clear problem solving, practical scientific judgement, and collaborative leadership. This role offers growth, meaningful impact and the chance to help GSK unite science, technology and talent to get ahead of disease together.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
Act as the single technical point of contact for the drug product portfolio, owning technical risk, decision-making and product knowledge.
Lead and deliver technology transfers to internal sites and external manufacturers, including transfer packages, training and readiness reviews.
Manage continued process verification, process performance qualification and change management to maintain product robustness and compliance.
Drive right-first-time execution of product qualification activities (e.g., PPQ/qualification readiness), managing appropriate governance through the relevant stage-gate forums as the program approaches PPQ, ensuring robust data, clear acceptance criteria and effective issue resolution.
Define and maintain product control strategy and technical risk assessments. Translate that knowledge into clear documentation for operations.
Support regulatory submissions and post approval inspections by providing technical input, comparability strategies and supporting documentation.
Manage cross-functional investigations, root cause analysis and corrective actions for complex deviations and quality events.
Why you?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals
Bachelor’s degree in a relevant scientific, engineering or technical discipline.
Minimum 10 years’ experience in pharmaceutical development, manufacturing or MSAT roles.
Demonstrated experience in technology transfer, process validation and product lifecycle technical leadership.
Practical knowledge of Good Manufacturing Practice (GMP) and regulatory expectations for drug product manufacture.
Experience applying risk assessment approaches, process control strategies and quality tools to maintain product performance.
Familiarity with regulatory dossiers and supporting health authority questions.
Strong written and verbal communication skills and experience working with multi-disciplinary teams.
Hands-on experience with oral solid dose drug product manufacturing.
Preferred Qualification
If you have the following characteristics, it would be a plus
Advanced degree (MSc, PhD) in a relevant scientific or engineering discipline.
Experience with Quality by Design, continued process verification and statistical process control.
Track record of leading complex technical investigations and delivering sustainable corrective actions.
Experience supporting regulatory filings, inspections and readiness activities.
Ability to lead improvement projects that demonstrate measurable technical or operational value.
Work Arrangement
This role is hybrid. You will be expected to visit manufacturing sites as required and spend regular time on site. Fully remote or permanent home-working arrangements are not available.
How to apply
We welcome applications from people with diverse backgrounds and experiences. If this role aligns with your skills and career goals, please apply. Tell us how your experience would help the team and what you hope to achieve at GSK. We look forward to hearing from you.
#LI-GSK
The US annual base salary for new hires in this position ranges from $125,250 to $208,750. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.Spanish Salary Range / Rango salarial en España: EUR 68,925 to EUR 114,875The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - [email protected]
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/
We are uniting science, technology and talent to get ahead of disease together. Our community guidelines: https://gsk.to/socialmedia
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