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- ...0% Remote Summary : We are seeking a proactive Validation Engineer with in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity. This is an on-site position that focuses on equipment...SuggestedRemote work
- About the DepartmentFor more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the...SuggestedWork at officeLocal area
$68 - $80 per hour
Reference: 630341Posted: 2026-08-27Location: Cambridge, MASalary: $68 - $80Company: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** Range: $68-80/hr *depending on experiencePosition Summary The PV Aggregate Reports Scientist is part of...SuggestedLocal areaWorldwide- Reference: 629568Posted: 2026-07-24Location: North Haven, CTCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** Engineer is responsible for providing daily support of multiple product families with specific regard to product...SuggestedWork at office
- ...required, DeltaV preferred.Prior experience leading or managing projects beneficial.CAPAs and deviations experience desired.Biotech/Pharma/Medical Device/Medical or biologics industry experience required.Ability to work independently and meet deadlines successfully....SuggestedFull timeRelocation package
$105k - $125k
...small companies or CMOsBackground in lean manufacturing / continuous improvementExposure to medical devices + adjacent industries (pharma, advanced manufacturing, etc.)Why This RoleHigh-impact opportunity to shape manufacturing processes for new and evolving productsDirect...Suggested- ...primarily on pharmaceutical accounts with secondary depth in MedTech, covering accounts that span both. This is a hybrid role. It combines pharma operating credibility across drug development, clinical operations, manufacturing and quality, and commercial functions with enough...SuggestedWork at officeImmediate startRemote workFlexible hours
- ...Execution Systems (MES) required, DeltaV is preferred.Experience leading projects and managing CAPAs and deviations.Background in biotech, pharma, or medical device industry.Strong attention to detail and ability to meet deadlines.Ability to work independently and on-site in...SuggestedFull timeRelocation package
- DescriptionThe Life Sciences & Technology Project Manager will lead and motivate a team in the day-to-day management of projects in the pharmaceutical, biotechnology, animal health and medical device industries. The Project Manager will be responsible for project safety...SuggestedContract workFor contractorsFor subcontractorWork at office
- Merck & Co. in Piscataway Township, New Jersey, is seeking a Group Leader to oversee the manufacturing process of pharmaceutical batches. The role demands strong leadership in validating production processes and ensuring compliance with safety standards. Ideal candidates...SuggestedShift work
- Ascendis Pharma, a dynamic biopharmaceutical company, seeks a Director of ICSR Management to lead the Global PV Operations team. You will oversee ICSR processing, regulatory adherence, and vendor oversight while shaping strategic plans with GPS leadership. Ideal candidates...Suggested
$190k - $205k
DescriptionAscendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.Here at Ascendis, we pride ourselves on exceptional...SuggestedFull timeTemporary workWork experience placementFlexible hours3 days per week- About the DepartmentThe Rare Disease organization leads all US Commercial efforts for Novo Nordisk’s Rare Disease portfolio. The Rare Disease portfolio includes medical treatments, customer solutions, and devices across multiple Therapy Areas including Rare Bleeding Disorders...SuggestedLocal areaNight shift
- ...and upcoming projects in the pipeline. Quality Control Responsibilities Must have at least 2-3 years of QC experience in biotech, pharma, or cGMP Conducts analytical/quality control testing in accordance with cGMP (21 CFR 211) for API and Drug products to ensure safety...SuggestedWork at office
- ...Position: Sr. SAP S/4 - SAP Lead FICO w/ SCM & Pharma Remote Duration: 6 Months Experience: 10+ Years Sr. SAP S/4 - SAP FICO with SCM & PHARMA LEAD functional Consultant - 100% Remote We are seeking an experienced Principal level SAP FICO Lead Functional...SuggestedRemote work
- ...communication skills and ability to work both independently and collaboratively in a cross-functional team environment.Experience in pharma or biotech environment is a plusSalary and Benefits:Frontage Laboratories offers a competitive compensation and generous benefits...Contract workTemporary work
- Reference: 630207Posted: 2026-08-18Location: Cambridge, MassachusettsCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** of Key Responsibilities *Works closely with the safety lead physician to analyze potential safety issues,...
- ...and other social benefits We care for our employees beyond the workplace and provide advice on caring for elderly relatives as well as offering counselling We promote sports and activities to improve our employees’ health #J-18808-Ljbffr medac pharma production GmbHRemote workFlexible hours
- Ascendis Pharma is seeking a Director of the ICSR Management Team in Palo Alto to lead pharmacovigilance operations and ensure timely ICSR processing in alignment with ICH-GCP and Health Authority requirements. The role oversees a team of ICSR leads, drives strategic planning...
- Pharma IT Business Analyst Proven experience working as a Business Analyst (BA) or Senior Business Analyst in Pharma GxP IT projects, preferably within the Pharmacovigilance domain. Strong understanding of end-to-end business processes and their alignment with IT solutions...
- ...Manufacturing, Quality Assurance, Facility Operations and Maintenance/Metrology, Engineering, EHS&S, and Quality Control to ensure that PCI PHARMA SERVICES assets are well engineered and maintained throughout their lifecycles.Prepare and execute factory acceptance testing (FAT)...Full timeFor contractors
- ...or with a strong statistical component, Masters or PhD preferred.5-7 years of experience in the application of medical statistics (pharma, CRO, academic).Willingness to engage with clients to understand and research problems and provide creative, business-orientated solutions...Full timeRemote work
$245k - $270k
...Kearney Healthcare & Life Sciences Practice Principal (Pharma R&D Strategy) As a Principal within Kearney's Healthcare & Life Sciences Practice, you will play a key role in driving the growth and development of our Pharma R&D Strategy offering. You will work closely...Immediate startHome officeFlexible hours- Description: JRS Pharma LP is seeking an experienced 3rd shift Maintenance Technician to join our growing U.S. Cedar Rapids, IA team as a key contributor to our maintenance operations. This role plays a vital part in ensuring the safe, efficient and precise maintenance...Hourly payFull timeFor contractorsWork experience placementNight shift
$80 per hour
...Quality Engineer Max. salary: 95K Medical Devices Industry Exp. is MUST (Pharma Exp. will NOT Help) Good Understanding of ISO 13485 Quality System Standards, FDA Quality System Regulations, ISO 14971, IEC 62366 and/or other international medical device standards...- Reference: 630046Posted: 2026-08-12Location: Mounds View, MNCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** you please confirm your top 3 skills sets required?Complaint handling experienceKnowledge of IMDRF or complaint coding...
- ...Contract: 9 months - based on performance and business needs Open for relocation candidate but first preference is local Active Pharma or medical device industry What are the top 3-5 skills, experience or education required for this position: Ability to...Contract workFor contractorsFor subcontractorLocal areaRelocationShift work
$110k - $135k
Reference: 628729Posted: 2026-08-06Location: South San Francisco, CaliforniaCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** OF RESPONSIBILITIES:The Senior Clinical Research Associate (Sr. CRA)/ Study Lead focuses on supporting...- Reference: 628708Posted: 2026-08-03Location: Brisbane, QueenslandCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** the OpportunityOur client is seeking an experienced and highly motivated Small Molecule CMC Principal / Director...Flexible hours
- About UsFounded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance...Full timeContract work


