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Packaging Operations Manager
2 months ago
We are seeking a highly skilled and experienced Packaging Supervisor to join our team at Cipla. As a key member of our packaging operations, you will be responsible for ensuring compliance with cGMPs, company policies, and regulatory requirements.
Key Responsibilities- Manage shifts and control activities in the absence of the Packaging Manager.
- Supervise activities and work performed on the floor.
- Support Line Leaders and other employees as needed.
- Maintain proper cGMP practices across all work areas.
- Responsible for working in all areas, including Pre-check and office duties.
- Responsible for working with Systech serialization system and SAP.
- Reduce time spent preparing lines for the next products.
- Train and educate employees as needed.
- Record In-process entries into respective documents.
- Check the Cleanliness of machines prior to or after use.
- Perform daily routine checkups and ensure safety measures are in place.
- Reduce time spent during changeovers.
- Enforce cGMP.
- Maintain full knowledge and a strong understanding of all SOPs and proper use of equipment.
- Be a point of contact for questions regarding procedures and expectations for employees.
- Serve as a leader and coach.
- Contribute to Standard Operating Procedure (SOP) writing in the technical area.
- Understand and operate all necessary equipment and instrumentation to perform activities.
- Maintain documentation in accordance with internal procedures and regulatory requirements.
- Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as follow current Good Manufacturing Practices (cGMP), comply with legal regulations, monitoring the environment.
- Perform other duties as assigned.
- One (1) to three (3) years of direct work experience in pharmaceutical packaging.
- Preference will be given to candidates with experience in generic pharmaceutical manufacturing and packaging.
- High School Diploma or GED is required. Bachelor's degree in Pharmaceutical Sciences or related field of study from an accredited college/university preferred.
- Must have 2 years cGMP work experience.
- Strong understanding of pharmaceutical packaging machines.
- Capable of conducting trouble-shootings.
- Capable of handling and participating in compliance and regulatory audits at the local and federal levels.
- Experience using SAP business systems and application is a plus.
- Must have 2 years cGMP work experience.
- Must be proficient in computer skills and software applications such as Microsoft Office tools.
- Bilingual in Spanish is preferred.
- Proficiently speak English as a first or second language.
- Ability to understand and analyze complex data sets.
- Knowledge of statistical packages is a plus.
- Knowledge of good manufacturing practices and good documentation practices preferred.
- Ability to read, write and communicate effectively.
- Self-motivated, with the ability to work in a fast-paced manufacturing environment and handle multiple tasks simultaneously.
- Excellent organizational skills with the ability to focus on details.
- Basic computer skills (Word and Excel) - Intermediate.
- Good basic math knowledge and excellent attention to details.
- Must be willing to work in a pharmaceutical packaging setting.
- Must be willing and able to work any assigned shift ranging from the first or second shift. The work schedule may be Monday to Friday.
- Must be willing to work some weekends based on business needs as required by management.
- No remote work is available.