Performs the assigned activities related to the equipment set-ups, changeovers equipment cleaning, and line clearance to achieve an efficient operation of the different processes and products yield maximizing.
Operates and understands the preparation, formulation and filling equipment functions and basic troubleshooting activities
Cleans, sanitize, and sterilize manufacturing area rooms and equipment.
Runs autoclaves to sterilize equipment to be used in the manufacturing process.
Performs CIP and SIP (Cleaning in Place and Sterilization in Place) of the tanks.
Performs integrity test of all filters used in the process before and after each use.
Receives, handle, verifies and weigh excipient and drug substance and or active ingredient to be used in the formulation process.
Executes the product formulation as per Batch record and Procedure instructions; this includes pH measurements and adjustments, yield calculations, and volume adjustment.
Performs sampling of bulk solutions as per batch record requirements.
Interacts with computer controlled equipment and processes.
Monitors critical process parameters and proactively takes necessary action to prevent process deviation and/or product losses.
Verifies calibration status of critical instruments before process operation.
Operates in an efficient manner of the manufacturing processes to maximize product yield of products.
Maintains housekeeping within controls and aseptic environments, according to procedures.
Performs systems integrity test such as isolators, ultra filtration skid, distribution systems, filters and gloves as required. Complete production documentation legible, error free and on time following good documentation practices.
Ensures the completeness and compliance of all required documentation during the manufacturing process.
Maintains inventory and request all necessary components and operating materials.
Receives, verifies all production records and transaction documents to be error free and in compliance with established procedures, including computer generated transactions.
Completes production documentation legible, error free and on time following good documentation practices.
Audits batch records and documentation, as required.
Assures that the Compounding equipment is in good working condition, clean, labeled, and calibrated and/or qualified according to applicable SOP’s before performing the formulation process.
Revises and improves procedures and develops new SOPs based on observations and experiences.
Provides assistance and supports to manufacturing related activities
Initiates, participates, and assists in resolution of quality investigations.
Assists in “on the job training” for new employees.
Participates in special projects and during audits and regulatory inspections as required.
Participates and assists in area validation and qualification activities.
Supports Environmental Monitoring Program by assuring samples collection on established timeframe.
Supports Annual Requalification Program by assuring plan execution on established timeframe.
Assists manufacturing activities in other areas within operations as required.
Follows up on progress of activities (e.g. documentation approval) with support departments and inform status to supervision, as requested by supervisor.
Performs GMP Safety and Environmental regulatory tasks required in the manufacturing area.
Maintains housekeeping within controls and aseptic environments, according to procedures.
Handles Hazardous and Non hazardous waste according to EHS procedures.
Attends to all mandatory training meetings for cGMPs, EHS and Company Policies.
Qualifications
High school diploma with, two (2) years of experience in Parenteral Manufacturing Process or three (3) years of experience in pharmaceutical manufacturing process. Bachelor's Degree in Microbiology, Biology and Chemistry can be consider.
Knowledge of preparation, formulation and filling processes.
Basic writing skills when completing area documentation.
Basic knowledge on Computerized, PLC control equipment, procedures and new scientific processes.
Ability to work with minimum supervision.
Ability to provide job training, theoretical and or On the Job, for new employees following the Parenteral Operations Department Qualification Curriculum.
Knowledge of all critical process parameters and their impact in product quality.
Knowledge in steam sterilization, depyrogenation, filtration sterilization, lyophilization and isolators technology. .
Understanding of Process Equipment set-up and able to perform it repeatedly and according to SOPs.
Ability to apply critical thinking to resolve complex issues.
Excellent leadership characteristics, accountability and commitment.
Team player and collaborating skills.
Knowledgeable in cGMPs, process area, documentation, safety, EHS and hygiene practices.
Skill in performing detailed tasks and documenting information.
Ability to enter data into a computer and perform complex process transactions.
Skill in accurate visual inspection (e.g. product and components defects)
Ability to read procedures and documents in English/Spanish Text (e.g. SOPs, Batch Records, etc.)
Skill in basic mathematical applications.
Skill in navigating through and performing transactions in mfg computer systems (HMI, hand held computers).
Strong organizational skills
Availability to work 12-hour shifts, overtime, weekends, and holidays.
Notes:
Responsibilities and accountabilities will vary for all positions and the scope of individual roles may not be limited to the contents of this position description.
This position will require the employee to work with chemical, radiological or biological agents that may be hazardous to health if mishandled (including agents who made potentially affect reproduction or the fetus or nursing infants). Employees will be required to follow all safety procedures and use personal protective clothing/equipment where specified.
About Us: Established in 2004, SPECTRAFORCE® is one of the largest and fastest-growing diversity-owned staffing firms in the US. The growth of our company is a direct result of our global client service delivery model that is powered by our state-of-the-art A.I. proprietary talent acquisition platform, robust ISO 9001:2015/ISO 27001 certified processes, and strong and passionate client engaged teams. We have built our business by providing talent and project-based solutions, including Contingent, Permanent, and Statement of Work (SOW) services to over 140 clients in the US, Canada, Puerto Rico, Costa Rica, and India. Key industries that we service include Technology, Financial Services, Life Sciences, Healthcare, Telecom, Retail, Utilities and Transportation. SPECTRAFORCE is built on a concept of “human connection,” defined by our branding attitude of NEWJOBPHORIA®, which is the excitement of bringing joy and freedom to the work lifestyle so our people and clients can reach their highest potential. Learn more at: http://www.spectraforce.com
Benefits: SPECTRAFORCE offers health benefits that include vision, dental, and pharmacy. Additional benefits offered to eligible employees include a 401K retirement plan with employer matching, a referral bonus program, and an EAP (Employee Assistance Program). SPECTRAFORCE provides unpaid leave as well as paid sick leave and vacation when required by law.
Equal Opportunity Employer: SPECTRAFORCE is an equal opportunity employer and does not discriminate against any employee or applicant for employment because of race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability or veteran status, or any other category protected by applicable federal, state, or local laws. Please contact Human Resources at benefits_pr@spectraforce.com if you require reasonable accommodation. At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $15.00/hr.
