Quality Control Analyst IV

Catalent

  • Chelsea, MA
  • Permanent
  • Full-time
  • 1 month ago
Quality Control Analyst IV - Tech Transfer TeamPosition Summary:Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.The Boston-area facility is Catalent’s global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America.Catalent Pharma Solutions is hiring a Quality Control (QC) Analyst IV who is a key analytical leader in a cGMP (Good Manufacturing Practices) laboratory capable of both clinical development and commercial testing. This analyst is both a mentor and trainer to team members and serves as a backup to QC management.This is a full-time on-site salaried position: Monday – Friday 8:00AM – 4:30PM.Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.The Role:
  • Operates analytical instrumentation (i.e. HPLC, UPLC, GC, UV-vis, FTIR, laser diffraction, Karl Fischer, etc.) for GMP testing of materials and product, for method transfers/validation, and for investigational purposes in a compliant and efficient manner
  • Performs data review and reporting (Certificate of Analysis (COA), reports, etc.). Statistically and critically analyzes data for trending and reporting in quarterly quality reviews and annual product reviews
  • Leads investigations for Deviations, Out Of Spec/Trend (OOS/OOT) results, and Product Quality Complaints
  • Monitors equipment and instrumentation to ensure efficient laboratory operations
  • Authors/Reviews/Approves controlled documents such as Standard Operating Procedures (SOPs), analytical test procedures, protocols, logbooks and checklists
  • Identifies and escalates both issues and opportunities for efficiencies on instruments and/or test executions; makes initial recommendations for possible solutions and/or corrective actions and implements solutions as appropriate
  • Trains and mentors team members on analytical instrumentation and material/product test methods. Leads team standup meetings and assists in laboratory scheduling
  • All other duties as assigned
The Candidate:
  • Bachelor’s Degree in Physical or Chemical Sciences (life sciences) required
  • Minimum of eight (8) years of experience in a cGMP regulated environment required
  • Experience in MDI/DPI analytical test methods (i.e. Andersen Cascade Impactor and Emitted Dose techniques) preferred
  • Extensive experience with executing GMP QC test methods, generating associated data packages, auditing data packages generated by others, troubleshooting instrumentation, trending data and statistical analyses required
  • Demonstrated ability to lead and/or author investigations to determine root causes of OOTs and/or OOSs according to cGMP standards required
  • Ability to troubleshoot and repair analytical instrumentation such as HPLCs and UPLCs preferred
  • Chromatography skills using Empower and/or ChemStation required
  • Critical understanding of the importance of documentation and data traceability required
  • Physical requirements: Individual may be required to sit, stand, walk regularly and occasionally lift 0-50 pounds
Why you should join Catalent:
  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Positive working environment focusing on continually improving processes to remain innovative
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • 152 Hours + 8 paid holidays
  • Several Employee Resource Groups focusing on D&I
  • Dynamic, fast-paced work environment
  • Community engagement and green initiatives
  • Generous 401K match
  • Company match on donations to organizations
  • Medical, dental and vision benefits effective day one of employment
  • Tuition Reimbursement – Let us help you finish your degree or start a new degree!
  • WellHub program to promote overall physical wellness
  • Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.personal initiative. dynamic pace. meaningful work.Visit to explore career opportunities.Catalent is an Equal Opportunity Employer, including disability and veterans.If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Important Security Notice to U.S. Job Seekers:Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.California Job Seekers can find our California Job Applicant Notice .

Catalent