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Quality Control Supervisor

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1 Vacancy
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Job Location drjobs

Devens, MA - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Who We Are:

At Veranova we believe people are our most important asset and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality compliance safety and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth and a desire to make a difference.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and nextgeneration therapeutics to improve and save the lives of patients.

Role Overview:

The QC Supervisor is responsible for managing a Quality Control (QC) team ensuring staff development timely support for manufacturing safety and GMP compliance. This role will also provide technical and compliance guidance to ensure the safety and productivity of the group embrace continuous improvement in all aspects of QC operations and oversee QC projects ensuring ontime completion with a high degree of quality.

Core Responsibilities:

  • Oversee and direct the work of Quality Control Chemists who perform GMP testing of raw materials intermediates and APIs in support of pharmaceutical manufacturing.
  • Interact with Production teams to assess Quality Control support needs and coordinates coverage for all shifts on assigned team.
  • Assign projects/ responsibilities to the QC team
  • Supervise QC personnel (including hiring decisions evaluations of performance and identification of training and development needs).
  • Owns and participates in Deviation and OOS investigations and pushes them toward closure
  • Develops improves and revises SOPs test methods and other GMP documentation.
  • Assures compliance of laboratory operations and contributes to laboratory organization
  • Leads the transfer of analytical procedures from the Analytical Development group as well as directly from the client sites.
  • Identifies and leads continuous improvement initiatives.
  • Communicates with internal and external clients.
  • Actively participates in quality and safety audits and walkthroughs.
  • Directs and advises the Quality Control group to achieve long and shortterm goals and objectives.
  • Provides guidance and direction to other staff to implement the company Quality vision
  • Always ensure the security and safe handling of all controlled substances. Strictly adhere to all Company and DEA regulations.
  • Ensure that waste is appropriately characterized labelled stored and disposed in compliance with all Company state and federal regulations. Work collaboratively with Environmental Health & Safety as appropriate.
  • Other responsibilities as assigned

Qualifications:

  • BS in Chemistry or equivalent with 5 years related experience OR MS in Organic Chemistry or equivalent with 3 years related experience.
  • Experience with common analytical techniques such as HPLC/UPLC GC NMR UVVis pH meter KF FTIR and Refractive index.
  • 3 years experience using chromatography (GC HPLC/UPLC)
  • 2 years experience with Quality records (e.g. deviations CAPA OOS)
  • 3 years Previous GMP experience
  • Experience with the creation and revision of GMP documents (e.g. test methods and SOPs)
  • Skilled in the use of Microsoft Office (e.g. Excel Word)
  • Ability to read analyze and interpret Englishlanguage chemical periodicals scientific journals and regulatory documents.
  • Ability to work independently and in a team environment.
  • Good written and verbal communication skills. Experience communicating effectively to management as well as peers and junior chemists.
  • Good timemanagement skills and dependability regarding daily tasks
  • Experience training other chemists on test methods and QC operations
  • Ability to write clear and concise technical reports.
  • Ability to make datadriven decisions

Preferred

  • Previous experience leading other chemists in a GMP environment
  • Familiarity with Laboratory Information Management Systems (LIMS)
  • Experience with Empower chromatographic software
  • Experience with statistical analysis of data
  • Experience with 5S

Our Commitment:

  • Health & Wellness: Comprehensive health & Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
  • Financial Wellness: Comprehensive total compensation package that includes competitive base salary Defined Contribution Pension program eligibility for performancebased bonuses and attractive 401(k) Plan with company match.
  • Professional Development: Opportunities for continuous learning through LinkedIn Learning workshops conferences and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
  • Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.

How to Apply:

At Veranova we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise.

We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients we encourage you to apply regardless of whether you meet every qualification listed.

If you are a veteran first responder or in the process of transitioning from service member to civilian life we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.

For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability you may submit your request by sending an email to in order to confirm your request for an accommodation. Please include the job number title and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Additional Information:

Applicants for this role must be authorized to work in the United States without further employer sponsorship.

Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.

Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.

If you have any doubts or concerns about the authenticity of a job posting please reach out to our HR department: (US) or (UK).

All your information will be kept confidential according to EEO guidelines.

Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age race color national origin religion sex sexual orientation gender identity and/or expression physical or mental disability genetic information citizenship marital status veteran status or any other characteristic protected by federal state or local law.

All applications are carefully considered and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.


Required Experience:

Manager

Employment Type

Full-Time

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