QA Operations Specialist

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title: QA Operations Specialist Classification: Full‑Time, Exempt/Salary, Professional Work Location: Fall River, MA Work Hours: General Shift: 8:30 AM – 5:00 PM (may vary based on business needs) Reports To: (Not specified) Salary Range: (Not specified) Job Purpose The purpose of the QA operations specialist (MDI) position is to monitor and ensure validation and qualification of facility, utilities, equipment and processes and to ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs). The role also provides guidance to QA associates. Duties and Responsibilities Review and approve qualification and validation protocols and reports including URS, FDS, FAT, SAT, DQ, IQ, OQ, and PQ, along with all supporting documentation. Review and approve User Requirement Specifications (URS) for equipment, systems, and utilities. Prepare, review, and approve Process Validation protocols and reports in accordance with lifecycle validation principles. Prepare, review, and approve Cleaning Validation protocols and reports for product contact equipment and manufacturing areas. Ensure all qualification and validation activities are planned and executed in alignment with applicable regulatory requirements (FDA, EU Annex 15, ICH Q8/Q9/Q10) and internal Standard Operating Procedures. Collaborate with cross‑functional teams (Engineering, Manufacturing, QC, Regulatory Affairs, IT, etc.) to support new projects, equipment implementation, and changes requiring validation. Provide Quality Assurance oversight during equipment commissioning, facility upgrades, and utility system qualification activities. Ensure risk assessments (e.g., FMECA) are performed and documented for validation and qualification activities. Maintain and manage the Validation Master Plan (VMP) and ensure periodic review and timely execution of requalification/revalidation activities. Participate in the investigation of deviations, out‑of‑specification results, and non‑conformances related to validation, and contribute to development and closure of effective CAPAs. Ensure validation and qualification documentation supports data integrity and is compliant with 21 CFR Part 11 for computerized systems. Maintain all validation lifecycle documents in accordance with company policies and cGMP expectations, ensuring traceability and audit readiness. Support internal and external audits, including FDA and other regulatory authority inspections, by providing relevant validation records, responses, and justifications. Education and Experience Bachelor’s degree in Pharmaceutical science or equivalent. Advanced vocational training or education in pharmaceutical manufacturing, industrial management, or related field of study from an accredited college/university is preferred. Minimum of 3 to 5 years’ experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment. Experience in MDI or combination products is preferred. Proficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP, TW and other business applications. Must be able to influence decision‑making and facilitate completion of work toward the achievement of the business plan and goals. Effective interpersonal relationship skills and the ability to work in a team environment. Proficiency in the English language to include usage, spelling, grammar, and punctuation. Must have current Good Manufacturing Practices (cGMP) knowledge. Must be a self‑starter and demonstrate initiative with seeking additional training or direction as needed. Must have strong organization and leadership skills (written, verbal, and presentation). Must be detail‑oriented with the ability to multitask and prioritize tasks with strict deadlines. Working Conditions This role works in a cGMP manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical manufacturing facility is required. The role may be assigned on a work‑shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Physical Requirements Work standing or walking unassisted for 75% or greater of an 8‑hour period. Unassisted lifting up to 10 kg may be required. Able to always wear appropriate personal protective equipment when required. Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8‑hour period. Professional and Behavioral Competencies Must be willing to work in pharmaceutical manufacturing and packaging quality assurance. Must be willing and able to work any assigned shift ranging from first or second shift. 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 available. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status. #J-18808-Ljbffr Cipla