Average salary: $122,277 /yearly
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- ...who range from small and emerging start-ups to large global pharmaceutical companies. The company is widely regarded as a leader in providing... ...seamless execution. A strong understanding of pharmaceutical validation, documentation practices, and relevant regulations is...SuggestedRemote jobFor contractorsFlexible hours
$157.6k - $236.4k
...Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate... ...formulation and process development, technical transfer and validation. The Associate Director of Drug Product Development will oversee...SuggestedContract workWork at officeRemote workWork from homeWorldwideFlexible hours$104.5k - $184.12k
...with international sourcing and 2nd source development Knowledge of supplier issue resolution, NOCs, Supplier tooling/equipment validations, and strategic sourcing Familiarity with capacity modeling and SOR management Familiarity with Subcontract Management Team (SMT)...SuggestedFull timeTemporary workPart timeWork experience placementRemote workRelocationFlexible hours3 days per week$90k - $120k
...more information, visit POSITION OVERVIEW We are seeking a Validation Engineer to assist with the development and execution of validation... ...Experience 4-7 years of experience within the biotech, pharmaceutical, or medical device industry. Knowledge and experience...SuggestedWork at officeRemote workWork visaFlexible hours- ..., process work instructions, engineering change orders, and MES configuration modeling.Leads equipment qualification and process validation tasks.Collaborates with cross-functional teams to evaluate and influence designs for manufacturability, cost reduction and business...SuggestedContract workApprenticeshipImmediate startRemote work
$22 - $30 per hour
...ability to work within an interactive and energetic workplace. Review process procedures, change orders, equipment specifications, validation plans, and reports. Performs research on technology, equipment and tooling to improve process quality, yield or cost....SuggestedHourly payInternshipWorldwideShift work$66.3k - $86k
...Cipla's U.S. Subsidiaries or Affiliates. Job Title : QA Validation - DPI FLSA Classification : Professional, Exempt... ....) on equipment and facilities and utilities associated with pharmaceutical manufacturing and drug product development. Job Overview...SuggestedFor contractorsWork at officeLocal areaRemote workMonday to FridayShift workAfternoon shift- ...Director, Clinical Science, Neuroscience TAU- Sleep Medicine in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize...SuggestedFull timeWork at officeRemote work
$104.5k - $184.12k
...international sourcing and 2nd source development • Knowledge of supplier issue resolution, NOCs, Supplier tooling/equipment validations, and strategic sourcing • Familiarity with capacity modeling and SOR management • Familiarity with Subcontract Management...SuggestedFull timeTemporary workPart timeWork experience placementWork at officeRemote workFlexible hours$120k - $157k
Scientist, Drug Safety (Pharmacovigilance) Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed... ...of high conviction programs with strong biological validation. Our asset-centric model offers a unique R&D logic that has...SuggestedFull timeFor contractorsFor subcontractorRemote work$88.38k - $106.19k
...associated with process equipment Commissioning, Qualification, and Validation Collaborate with Quality, Mfg Managers, Plant Engineering,... ...Qualifications: High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience...SuggestedWork experience placementRemote workFlexible hoursShift work- ...Demonstrates ability to perform competencies and perform activities as outlined in the Pharmacist Authorities policy. Provides pharmaceutical care according to standards established by Scripps Health Pharmacy, to assigned group of patients. Reviews and evaluates...SuggestedFull timeRemote workRelocation packageShift work
- ...associated with process equipment Commissioning, Qualification and Validation. Collaborate with Quality, Mfg Managers, Plant Engineering,... .... Basic Qualifications: High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience Or...SuggestedWork experience placementRemote workFlexible hoursShift work
- ...improvement. Required Skills for the Pharmacovigilance Specialist: 5+ years of experience working in Healthcare/Pharmaceutical Case Management (Adverse events) Strong experience writing/training on product procedures Experience working with FDA...SuggestedRemote work
- ...associated with process equipment Commissioning, Qualification and Validation. Collaborate with Quality, Mfg Managers, Plant Engineering... ...Qualifications: High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience...SuggestedWork experience placementRemote workFlexible hours
- ...Summary The clinical pharmacist, is a professional with knowledge and proficiency in pharmacy practice including pharmaceutics, pharmacokinetics, pharmacodynamics and pharmacotherapeutics. The incumbent is responsible for analyzing real and potential drug-related medical...Permanent employmentTemporary workWork experience placementSeasonal workLocal areaRemote workTrial periodRelocation packageMonday to Friday
$64k - $90k
...and metrics reporting. * Provide remote support to Global Metrology. Perform review of calibration work, supplier certificates, or validation documents. What you'll bring: * Bachelors or Associates Degree in a technical discipline or equivalent with 6+ years' experience...Temporary workLocal areaRemote workWorldwideFlexible hours$27.95 - $40.7 per hour
...assigned CAP proficiency testing 6. Participate in quality assurance activities, such as assisting with new assay and equipment validation and periodic updates to standard operating protocols Qualifications Education: Bachelors Degree in Biological...Hourly payRemote workRelocation packageShift workDay shift- ...Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize...Full timeWork at officeRemote workNight shift
$139.1k - $231.9k
...it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance... ...audit readiness.* Collaborate on equipment installations, validations, and preventative maintenance, and lead budget planning for...Permanent employmentH1bLocal areaVisa sponsorshipWork visaRelocation packageShift workWeekend workAfternoon shift- ...limited to medication guidelines, clinical pathways, core measures, education, and policy development. Provides collaborative pharmaceutical care with the respective specialized teams in identified patient care areas. Reviews and evaluates individual drug orders...Full timeRemote workRelocation packageShift work
- ...developmental products, managing a team, and collaborating cross-functionally. Ideal candidates will have 15+ years of experience in the pharmaceutical industry, focusing on pharmacovigilance, safety data analysis, and team leadership. The position allows for remote work within...Remote work
$22 - $30 per hour
...Supporting Manufacturing Engineering in duplicating manufacturing and test fixtures, as well as developing and executing IQ, OQ, and PQ validation activities. Conducting basic PCB troubleshooting, analyzing data for trends, and preparing and presenting findings. The Intern...Hourly payInternshipWorldwideShift work$139.48k - $169.01k
...other functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering. Support equipment and systems validation activities, including review of equipment qualification documents, drafting user requirements and participating on impact...Hourly payFull timeTemporary workPart timeSummer workImmediate startRemote workFlexible hoursShift work$22 - $30 per hour
...ability to work within an interactive and energetic workplace. Review process procedures, change orders, equipment specifications, validation plans, and reports. Performs market research on relevant topics. Qualifications Minimum Knowledge & Experience Required for the...Hourly pay- ...sciences companies connect with HCPs and improve lives. Our services span the entire product life cycle for our clients in the pharmaceutical and medical device industry. We are currently seeking an Event Planner to join our remote team. The Event Planner is responsible...Work experience placementWork at officeLocal areaRemote workWeekend work
- ...has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that...Contract workLocal areaRemote workWork from home
$80k - $100k
(on-site) Position: Pharmacovigilance Supervisor Location: New Jersey (on-site) Salary Range: $80,000 to $100,000 per year About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With...Contract workTemporary workWorldwideFlexible hours- ...sciences companies connect with HCPs and improve lives. Our services span the entire product life cycle for our clients in the pharmaceutical and medical device industry. This position is responsible for coordinating all aspects of multiple medical education programs...Contract workWork experience placementRemote work
- Pharmacovigilance & Drug Safety Specialist (PharmD) Bring your clinical lens to the world of drug safety and reporting. Responsibilities Analyze adverse event reports and clinical trial safety data. Prepare regulatory submissions (e.g., MedWatch, PSURs). Collaborate...Remote work



