Company Description
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.
Job Description
The principal responsibilities of the Production Supervisor include supervising the daily activities of the Production staff assigned to their shift, scheduling equipment maintenance as required, monitoring production processes to ensure the cost effective and timely delivery of product fit for its intended use to meet customer needs and commercial schedule.
Key Responsibilities / Accountabilities Effectively utilizes manpower, materials and equipment to produce quality products fit for their intended use, in a safe manner and at the optimum level of productivity to maximize business unit profitability.
Ensures that all work is performed in compliance with Company SOPs, FDA CGMPs, DEA regulations and all local, state and federal regulations regarding safety, health and the environment.Ensures that both the facility and pharmaceutical systems documentation are maintained in compliance with Company and FDA/CGMP and DEA regulations and practices.Ensures that waste is appropriately characterized, labeled, stored and disposed in compliance with all Company, state and federal regulations.
Works collaboratively with Environmental, Health & Safety, as appropriate.
Assures all production/support equipment is in proper operating condition and that all production equipment is appropriately labeled with a current status tag.
Works collaboratively with Maintenance, as appropriate.Ensures the security and safe handling of all controlled substances at all times.
Strictly adheres to all Company and DEA regulations.Promptly reports all incidents in the correct manner, according to procedure and completes investigations as necessary.Promotes a positive work environment by maintaining a safe work area and ensuring that their team members have the knowledge, skills and appropriate tools to perform their assigned duties and a thorough understanding of their performance expectations.
Administers Company policies fairly and consistently.
Write and suggest improvements for Standard Operation Procedures (SOPs), Master Batch Records (MBRs) and other related GMP documentsResponsible for contributing to audit readiness and for participating in quality and safety audits with FDA, other Regulatory Agencies, internal audits, and customers, as needed.Responsible for planning, delegating, and monitoring assigned work tasks that are completed during shifts.
Accountable for the growth and discipline of team members. Qualifications AA Degree with a minimum of 3-5 years API experienceHigh School Diploma with a minimum of 5-7 years pharmaceutical experience Experienced in cGMP manufacturing Experience with Microsoft Office and other job-related softwareGood written and verbal communication and interpersonal skillsAbility to independently apply scientific and/or technical principalsTeam leadership or supervisory experienceSolid understanding of GMP and FDA regulationsGood mechanical aptitude Additional Information
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.
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For more information about how your personal data is used please view our privacy notice.