What are the responsibilities and job description for the Inspector/Labeler position at Piramal Pharma Ltd?
Job Description
Business: Pharma Solutions
Department: Operations
Location: Lexington
Job Overview
Reporting to the Process Technician Supervisor, the primary purpose of the Inspector/Labeler role is to perform visual inspection, labeling, and packaging activities for finished product, according to Good Manufacturing Practices (GMP) and site specific Standard Operating Procedures (SOP).
Reporting Structure
This position reports to the Process Technician Supervisor.
Shift
Days
Key Responsibilities
In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.
Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.
Equal employment opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.
We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.
About The Team
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.
Business: Pharma Solutions
Department: Operations
Location: Lexington
Job Overview
Reporting to the Process Technician Supervisor, the primary purpose of the Inspector/Labeler role is to perform visual inspection, labeling, and packaging activities for finished product, according to Good Manufacturing Practices (GMP) and site specific Standard Operating Procedures (SOP).
Reporting Structure
This position reports to the Process Technician Supervisor.
Shift
Days
Key Responsibilities
- Preparation of Line clearances for inspection, labeling and packaging processes.
- Clean and disinfect any inspection/labeling equipment and rooms, preparing of rooms and equipment.
- Cleaning of SS trays post inspection.
- Maintain inspection, labeling and packaging areas clean and organize at all times.
- Inspection of both liquids and freeze dried products.
- Labeling of both liquids and freeze dried products.
- Packaging of both liquids and freeze dried products.
- Request QA AQL.
- Transfer Materials and/or components from in and out of the production area and back into the WHS.
- Daily verification of room temperature and humidity chart recorders.
- Read, understand, and comply with Good Manufacturing Practices and Standard Operating Procedures.
- Maintain and review completed production documentation (batch records, log books, etc.) for quality and cGMP compliance.
- Initiate appropriate action when process deviations occur.
- Other duties as assigned by production supervisor.
- High School education or equivalent
- Minimum 1-year experience working with a manufacturing/industrial environment, pharmaceutical manufacturing preferred
- Experience performing visual quality checks on products within a manufacturing environment
- Prior knowledge and/or ability to understand and follow job related regulatory requirements (cGMP, OSHA, FDA)
- Keen attention to detail and ability to read, interpret and follow written instructions
- Team player committed to quality and working effectively with others
- Track record of consistent attendance and overall reliability
In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.
Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.
Equal employment opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.
We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.
About The Team
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.