Packaging Supervisor -3rd Shift
Listed on 2025-12-07
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Manufacturing / Production
Packaging Engineer, Pharmaceutical Manufacturing
Packaging Supervisor - 3rd Shift at Cipla USA
PurposeInva Gen Pharmaceuticals, Inc. is searching for an experienced Packaging Supervisor who will supervise packaging operators and oversee production processes in the absence of the Packaging Manager. The Packaging Supervisor ensures compliance with cGMP, Inva Gen’s policies, standard operating procedures, and FDA requirements. The incumbent will serve as a key resource for conducting product complaints, supporting packaging, and packaging components within approved procedures and regulatory requirements.
Job Duties- Managing shifts and control activities in the absence of the Packaging Manager.
- Supervising activities and work performed on the floor.
- Supporting Line Leaders and other employees when necessary.
- Maintaining proper cGMP practices across all work areas.
- Responsible for all Pre-check and office duties.
- Working with the Systech serialization system and SAP.
- Reducing time spent preparing lines for the next products.
- Training and educating employees when necessary.
- Recording in-process entries into respective documents.
- Checking the cleanliness of machines prior to or after use.
- Performing daily routine checkups and ensuring safety measures are in place.
- Reducing time spent during changeovers.
- Enforcing cGMP.
- Maintaining full knowledge and a strong understanding of all SOPs and proper use of equipment.
- Being a point of contact for questions regarding procedures and expectations for employees.
- Serving as a leader and coach.
- Contributing to SOP writing in the technical area.
- Operating all necessary equipment and instrumentation to perform activities.
- Maintaining documentation in accordance with internal procedures and regulatory requirements (i.e., GMP, SOPs).
- Following strict internal protocols and SOPs as well as current Good Manufacturing Practices (cGMP), comply with legal regulations, and monitor the environment.
- Performing other duties as assigned.
- One to three years of direct work experience in pharmaceutical packaging, with preference for experience in generic pharmaceutical manufacturing and packaging.
- High School Diploma or GED required;
Bachelor’s degree in Pharmaceutical Sciences or related field preferred. - Minimum two years of cGMP work experience.
- Strong understanding of pharmaceutical packaging machines.
- Capability to conduct troubleshooting.
- Participation in compliance and regulatory audits at local and federal levels.
- Experience using SAP business systems and applications is a plus.
- Proficiency in computer skills and software applications such as Microsoft Office.
- Bilingual in Spanish preferred.
- Proficient in English as first or second language.
- Ability to understand and analyze complex data sets.
- Knowledge of statistical packages is a plus.
- Knowledge of good manufacturing and documentation practices preferred.
- Excellent communication skills, both written and verbal.
- Self‑motivated with the ability to work in a fast‑paced manufacturing environment and handle multiple tasks simultaneously.
- Excellent organizational skills with attention to detail.
- Basic computer skills (Word, Excel) – intermediate.
- Good math skills and meticulousness.
- Willingness to work in a pharmaceutical packaging setting.
- Willingness to work any assigned shift, ranging from the first or second shift.
- Required to work some weekends based on business needs.
- No remote work available.
Applicants who receive a conditional offer must satisfactorily complete pre‑employment drug testing.
Disclaimer on Pay RangesThe salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and a bonus program based on performance and company results.
EEO StatementCipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact c
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