Catalent Pharma Solutions Inc

Manager, Molecular & Cellular Biology

Catalent Pharma Solutions Inc$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree with over 5 years of experience in relevant techniques
  • 2+ years of management experience in a technical field
  • In-depth knowledge of instrumentation and data interpretation in a specific area
  • Experience in drug development lifecycle support
  • Strong written and verbal communication skills for diverse audiences
  • Ability to simplify complex concepts for non-experts
  • Proven leadership in resolving challenging discussions with clients

Responsibilities

  • Supervise method development and validation processes in Molecular and Cellular Biology
  • Plan and execute analytical work per client contracts and technical agreements
  • Serve as Project Technical Lead when required
  • Oversee computer system validation and compliance of lab equipment
  • Ensure adherence to cGMP practices within the team
  • Guarantee integrity and quality of analytical data by following SOPs
  • Monitor project timelines and budgets while facilitating communication across teams

Benefits

  • Competitive medical benefits and 401K
  • 152 hours of PTO plus 8 paid holidays
  • Fast-paced and dynamic work environment
  • Engagement in Continuous Improvement Processes
Full Job Description

Manager, Molecular & Cellular Biology

Position Summary

  • Shift: Monday – Friday 8am – 4:30pm
  • 100% on-site

The Manager in Molecular and Cellular Biology is primarily responsible for managing various sub-teams comprised of a Group leaders, Scientists and Associate Scientists. Their responsibilities will include serving as technical experts on projects, act as liaison between client and Catalent technical team, coaching and mentoring group leaders, HR activities (e.g., performance reviews, time entry approval, PTO approval, salary adjustments, etc.), supporting client audits/visits, and communicating with cross-functional teams on analytical activities for Biopharma product development under cGMP regulatory guidance for Large Molecules/Biologics product development.

The role:

  • Supervise and manage various method development, method evaluation/feasibility, method transfers, method verifications, qualifications and validations, stability study and adhoc sample testing in Molecular and Cellular Biology.
  • Plan, prioritize, organize, and execute the conduct of analytical work within the Molecular and Cellular Biology Laboratory in accordance with the requirements of the client contract and/or technical agreement.
  • Serve as back up Project Technical Lead and could also serve as Technical Lead on projects pertaining to Molecular and Cellular Biology.
  • Manage and lead computer system validation activities, as required. Ensure various instruments/Equipment in the group are in compliant status.
  • Ensure cGMP practices are implemented and followed by the group and self.
  • Assure the integrity and quality of analytical data produced by ensuring staff are adhering to all relevant in-house and client SOPs and methodologies and following the requirements of GMP.
  • Monitor and manage projects and maintain project timelines and budget.
  • Communicate effectively with clients, auditors, peers, and Directors to facilitate the smooth conduct of project activities.

The candidate:

  • A minimum of a Bachelor’s degree with > 5 years of relevant experience in department specific techniques with > 2 years of management experience
  • Applies knowledge of the principles, theories, and concepts applicable to a wide range of work in a discipline (e.g., Biology, Chemistry, Biochemistry) and broad knowledge of principles and concepts in other disciplines.
  • In-depth knowledge in instrumentation, theory, data interpretation and applications in at least one technical area. Can assess new technologies and their impact on Catalent offerings
  • Experienced in most aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones
  • Excellent written and verbal communications skills with internal and external customers, colleagues, and supervisor.
  • Ability to communicate complex technical information to non-technical audiences
  • Able to lead difficult discussions with customers and drive the to an acceptable resolution

Why you should join Catalent:

  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Founded
2007

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