Packaging Supervisor
Edison, United States, New Jersey, 00000
Who we are
The opportunity
Supervise packaging department activities and personnel while ensuring full compliance with cGMP, SOPs, EHS, DEA, Union Shop Floor Requirements, Company Policies, and applicable regulatory requirements.
How you’ll spend your day
• Supervise the filling and packaging of solid dose products.
• Direct, coordinate, and support Union employees in the Packaging Department.
• Ensure all departmental activities are performed in accordance with cGMP requirements.
• Write, revise, and update SOPs pertaining to packaging operations and review updates with employees.
• Train packaging personnel on revised procedures, new equipment, and new applications.
• Maintain a strong focus on quality, safety, and efficiency, continuously evaluating work practices for improvement opportunities.
• Supervise and support the Printed Materials area, including bottle labels and outserts.
• Perform Packaging Batch Record Reviews and process work orders in the ERP system.
• Initiate and support Change Control requests related to Master Packaging Records (MPRs) and SOP updates.
• Support Master Packaging Record review activities for accuracy and compliance.
• Ensure security, accountability, and proper inventory control for materials and finished goods.
• Recommend process improvements to increase departmental efficiency.
• Ensure adherence to packaging standards and administer disciplinary action when required.
• Work within the approved annual operational budget.
• Conduct thorough investigations of packaging deficiencies and document findings appropriately.
• Collaborate with cross functional departments to support production requirements.
• Ensure OSHA standards are maintained by promoting and enforcing a clean and safe work environment.
• Identify and prevent health and safety issues (dress code, hygiene, equipment condition, etc.); report and document accidents/incidents per proper procedures.
• Provide input and maintain accuracy within the Inventory Control (ERP) system.
• Perform other duties as assigned by the Manager/Director.
• Build accountability on the shop floor by following Union work rules and issuing disciplinary actions when appropriate.
• Maintain the Employee Time Card System, including work hours, vacation, leave of absence, and overtime control.
• Identify and implement production process improvements to enhance quality, reduce cost, and improve safety.
• Must be able to read, write, speak, and comprehend English.
• Actively participate in OPEX and Lean Manufacturing initiatives.
• Routinely inspect packaging lines, equipment washrooms, clean equipment storage areas, and material staging areas to ensure compliance.
Your experience and qualifications
- High School diploma required; BS/BA in a science or related field preferred.
- 2–5 years of supervisory experience within a pharmaceutical manufacturing or packaging environment.
- Solid dose packaging experience is highly preferred.
- Knowledge of Solid Oral Dose packaging equipment and familiarity with various packaging machinery (tablet/capsule fillers, cappers, labelers, etc.).
- Ability to understand and operate vision inspection systems (e.g., Optel) and support setup and troubleshooting.
- Strong working knowledge of pharmaceutical cGMP requirements.
- Demonstrated ability to adapt to change, support multiple shifts when necessary, and manage shifting priorities.
- Proven ability to follow production schedules, meet deadlines, and learn new systems and operational processes.
- Excellent verbal and written communication skills, with effective interpersonal abilities.
- Self-motivated, team-oriented, and capable of working independently.
- Proficiency with Microsoft Office (Word, Excel), TrackWise, Document Control Systems, and ERP systems.
- Physical ability to lift up to 25 lbs., and walk, stand, or sit as needed.
How We'll Take Care of You
We offer a competitive benefits package, including:
- Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
- Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
- Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
- Life and Disability Protection: Company paid Life and Disability insurance.
- Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.
The total compensation may also include restricted stock units and discretionary awards, depending on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to disabilityassistance@tevapharm.com with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address.
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Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.