PURPOSE OF THE ROLE
The primary purpose of the role is to support the Operations team with documentation and processes to meet production needs.
Assist engineers in developing, building, or testing prototypes/new products, processes, validations or procedures.
Adhere to all applicable regulations, policies, and procedures for health, safety and environmental compliance
Monitor and adjust production processes or equipment for quality and productivity gains.
Provide training to operators as needed
Assist in providing information to Transfer Tech and Validation Crew on investigations
Assist/Support OPS Management and QA: Open, Follow up, and close deviations, CAPAs, QA Investigations and TA's.
Assist work team in the achievement of goals/commitments and achieves own goals/commitments regardless of obstacles
Update Operation's SOP's, as needed, and perform periodic review of procedures.
Assist in driving continuous improvement activities
Moderate to heavy lifting and manual material handling; bending/twisting to manipulate equipment and chemicals, occasional lifting up to 50 pounds
Frequent long periods of standing, walking
Must use hands to handle, feel, reach, type or operate objects or controls
Must be able to pass a respirator fit test and wear a respirator as needed
Ability to work in a high demand manufacturing setting.
Within the manufacturing core, the employee will on occasion work with toxic and cytotoxic materials within a safe manner.
Position may require extended hours including evenings and weekend
Personal protective equipment including safety glasses, lab coats, gloves, specialized clothing including laboratory uniform and appropriate shoes may be required in areas associated with this position.
EQUAL EMPLOYMENT OPPORTUNITY
Piramal Pharma Solutions is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, 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, or other applicable legally protected characteristics.
KNOWLEDGE AND SKILLS
At least 2 years working within a manufacturing environment, cGMP/pharmaceutical manufacturing preferred
Operational capacity working with batch records
Experience with technical writing
Demonstrated ability to work collaboratively with others
Excellent oral/written communications
Skilled at conflict resolution and decision making
Ability to read and follow written instructions, keen attention to detail
Excellent organizational skills and ability to multi-task
Piramal Enterprises Ltd.