Qc supervisor (2nd shift)

Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented 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 next-generation therapeutics to improve and save the lives of patients. Every role at Veranova plays a part in delivering an exceptional customer experience through ownership and integrity.

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. Provide technical and compliance guidance to ensure the safety and productivity of the group. Oversee QC projects, ensuring on-time completion with a high degree of Quality. Provides leadership to the group through effective communication, coaching, training, development. Ensure staff acts in accordance with company policies and other applicable regulatory requirements (e.g. GMP, ICH, OSHA). Responsible for daily scheduling and prioritization so staff is aligned to most effectively achieve QC goals.

Schedule: Monday-Friday 3PM-12AM

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.
• Supervise QC personnel (including hiring decisions, evaluations of performance, and identification of training and development needs).
• May be required to perform analysis and report results in accordance with cGMP & GLP requirements.
• Owns and participates in Deviation and OOS investigations, and pushes them toward closure.
• Develops, improves, and revises SOPs, test methods, and other GMP documentation.
• 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.
• Communicate with internal and external clients.
• Actively participates in quality and safety audits and walkthroughs.
• Performs work following all state and federal regulations, including but not limited to GMP, DEA, FDA, etc.
• 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, UV-Vis, 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 training other chemists on test methods and QC operations. Previous experience leading other chemists in a GMP environment preferred. Experience with Empower chromatographic software preferred.

Salary Range:

The salary range for this role is $100,000-$110,000. This range represents a good-faith estimate of the compensation we expect to offer for this position at the time of posting. Actual compensation will be based on factors such as relevant experience, skills, qualifications, and internal equity. In exceptional cases, compensation may exceed the stated range. All full-time employees are eligible to participate in our annual incentive bonus program. Bonus targets vary by career level and are based on individual and company performance.

Our Commitment:

• Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
• Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.
• 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 welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don’t meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.

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. Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com. Legitimate LinkedIn communications will only come from active Veranova employees. Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number). Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks). If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: pharm.hr@veranova.com. 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.