SUMMARY:
Responsible for ensuring that all products, processes, and systems meet regulatory and quality standards through rigorous testing and analysis. Collaborate with cross-functional teams to design, develop, and execute validation protocols, and generate validation reports to ensure compliance with regulatory requirements.
Work Schedule: Monday - Friday 8am-5pm, OT required per project needs
JOB QUALIFICATIONS:
- B.S. (or equivalent 4-year degree) in Engineering or Science Related Field
- Minimum of 5 years validation experience supporting pharmaceutical cGMP manufacturing and/or technical support operations
- Experience with Liquid, Solids, Medical Devices and Semisolid Dosage Forms
- Experience authoring, executing and summarizing validation qualification protocols
- Experience with Cleaning Validation including swabbing and reinstate sampling
- Regulatory inspection experience with external regulatory authorities
- Knowledge of the principles and application of statistical analysis preferred
- Technical writing and attention to detail required
- Trained and experienced on Validation (Product Life Cycle), Start-Up, Equipment Evaluation, Selection and Commissioning
- Extensive knowledge on Technical Investigations and Product/Process Development/Optimization.
- Experience in administrative techniques, Vendor Qualifications
- Knowledge of the principles and application of cGMP guidelines related to validation activities
- Time management and ability to handle multiple tasks on time
- Relies on extensive experience and judgment to plan and accomplish goals
- Computer literate • Strong conflict resolution skills
- Strong communication skills - verbal and written
- Strong collaboration and teamwork
- Willingness in traveling
POSITION RESPONSIBILITIES:
- Establish validation standards, develop testing protocols, prepare equipment, document test results and maintain records for later analysis
- Validate new and re-validate as appropriate existing equipment used in OTC/Rx manufacturing, packaging, compose reports and make adjustments to equipment or processes that require improvement
- Evaluate, implement and monitor processes, operating systems, critical utilities, manufacturing and packaging equipment in accordance with appropriate regulatory agency validation requirement and current industry practices
- Create/edit/maintain necessary documentation that pertain to the Evaluation of the Process Qualification PPQ/Manufacturing & Packaging Equipment Qualification and the Status of the Critical Utilities (HVAC, USP DI Water Compress Air System) as well as any other utilities that affect directly the Critical Products Attributes
- Evaluation of the Critical Utilities, Manufacturing and Packaging Equipment calibration and maintenance monitoring during the execution of these systems Qualification
- Evaluation of existing and/or creation of Cleaning, Operation Procedures for the critical utilities, manufacturing and packaging equipment.
- Assess the availability of raw materials and their impact in a specific manufacturing process not only from the process influence but also from the safety and environmental influence of the facility related to this material
- Support the conversion during the “Scale Up” of any Manufacturing Process that has been developed at a small-scale process into commercially viable large-scale commercial operations
- Coordinate and responsible of all New Molecules transfers from R&D bench/pilot size to the manufacturing.
- Monitor and improve the efficiency, output and safety of manufacturing processes through observations and measurements as well as by collecting and interpreting data from other technical and operating personnel
- Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols
- Work closely with other specialists (including scientists) for quality control of raw materials.
- Measure instrument or software performance to determine if tools are performing as described for temperature mapping, and calibration activities
- Provide validation support for Computerized Systems including Automation and Laboratory Equipment and qualification / validation activities of Primary / Secondary manufacturing operations
- All other duties, as assigned
PHYSICAL REQUIREMENTS:
- Assume responsibility for safety/environmental issues during an ongoing performance qualification of a manufacturing process
- Must be able to lift and carry light loads as necessary in conducting testing
- Weekend or long hours based on testing schedule
- May involve standing for long periods of time
- Must be able to wear proper gowning and PPE in manufacturing areas as required to meet GMP and/or OSHA requirements