Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients.
As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being.
Reaching People. Touching Lives.
Job purpose
The main responsibility for this position is to provide support for site-wide Quality Assurance Programs including GMP Documentation and Change Control to meet SUN Pharma, Canadian and FDA GMP requirements.
This position acts to oversee the processing of GMP Documents including revisions, posting, archival as well as maintenance and storage of GMP documents at the SPCI QA Documentation Center and Third-party Documentation Storage Facility.
Duties and responsibilities
- Organize and coordinate the archival, retention and retrieval of GMP Documentation generated at SPCI.
- Support Regulatory Inspections and Customer Audits through the timely retrieval of Documentation
- Support revision and posting (making effective) of Quality Control Documents (eg Test Methods, Specifications) and Master Production Documents as per assigned Change Control tasks in a timely manner
- Facilitate communication with stakeholders required for completion of Change Control tasks within assigned due date
- Support QC, QA and RA Departments by updating specifications, test methods required for regulatory submission as assigned and monitor and support the further implementation when approved by the Agency
- Support Production and QA Incoming Departments with maintenance of active and archived Engineering, Packaging specifications and ArtWork electronic packets.
- Maintain and regularly review GMP Documentation inventory to assure timely closure of document requests, timely transfer of documents for archival at a third-party storage facility and provide support for timely GMP document destructions
- Act as a backup for Specialist, QA (Documentation) as per the business needs
- Generate, gather and analyze data to support specified Quality Systems: Documentation and Change Controls
- Generate reports associated with the specified Quality Systems: Documentation and Change Controls
- Perform assigned tasks for implementation of new Documentation related Software systems: eg EDMS, BRMS, as required.
- Perform assigned actions related to SUN global projects for documentation updates: eg rebranding of GMP Documentation, ArtWork Rebranding.
- Participate in Internal Quality Audit and Internal Self-Inspection Program as assigned
- Complete required Department trainings within assigned due date
- Identify and report issues required improvements in the area of expertise related to the job duties and propose the enhancement to support the efficiency.
- Work with other departments to proactively build quality into the processes and systems
- Perform responsibilities in a GMP compliant and safety conscious manner
- Other duties as assigned
Additional responsibility (Only applicable to customer facing roles)
Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day
Qualifications
- Bachelor’s Degree or a College Diploma in a Science related discipline
- Previous experience in the pharmaceutical Industry in a Quality / Documentation Coordination Role is preferred
- High Proficiency in MS Word and Excel
- Sound knowledge of Health Canada and FDA regulations
- Good verbal and written communication skills
- Ability for Critical thinking and analyzing
- High attention to details and ability to stay focused when multitasking
- Ability to establish and prioritize daily work schedules in a fast-paced environment.
- Ability to work independently and under minimum supervision.
- Ability to identify discrepancies, deviation form procedures, issues related to completion of tasks and brought to the attention of management with logic, data and corrective measures proposed.
- Well-developed interpersonal and teamwork skills
Working conditions
- Ability to manage work under fast-changing priorities
- Numerous and varied responsibilities demanding attention and detail
- Working in general office and QA Documentation Centre
- Some physical lifting and carrying document boxes, as required
Physical requirements
NA
Direct reports
NA
This posting is for an existing vacancy.
The presently-anticipated base compensation pay range for this position is $56,500 to $71,000. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; RRSP savings plan; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.
The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, ethnic origin, citizenship, ancestry, sex, age, marital status, family status, physical or mental disability, gender identity, gender expression or any other ground protected by applicable human rights legislation.
The Company uses artificial intelligence to screen, assess or select applicants.
Notice to Agency and Search Firm Representatives: Sun Pharmaceuticals Industries, Inc. (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
