Cipla, a global pharmaceutical company with a strong presence in South Africa, is currently offering a variety of career opportunities for individuals looking to make a difference in the healthcare industry. Renowned for its commitment to affordable healthcare and innovative pharmaceutical solutions, Cipla is dedicated to improving the quality of life for people around the world. This article explores the diverse vacancies available at Cipla, highlighting the roles and opportunities to join a leader in the pharmaceutical field.
QA Operations Specialist – Fall River, MA, USA
Key Information
Details
Job Title
QA Operations Specialist
Location
Fall River, MA, USA
Work Hours
General: 8:30 AM – 5:00 PM (may vary based on business needs)
Reports To
QA Manager
Job Purpose
Ensure validation and qualification of facility, equipment, processes, and product quality
Duties and Responsibilities
Review batch manufacturing/packaging records, engineering records, manage non-conformances, and provide quality updates. Lead shop floor quality activities.
Education and Experience
Advanced vocational training or Bachelor’s degree preferred, 5 years of QA experience in cGMP, MDI or combination products experience preferred.
Competencies
Proficient in Microsoft Office, SAP, cGMP knowledge, strong organization, leadership, and communication skills.
Physical Requirements
Work standing/walking 75% of the time, unassisted lifting up to 10 kg.
Working Conditions
cGMP environment, use of PPE required, work with solvents/powders, shift-based work possible.
How to Apply
10 Dec2024
Senior Operator – Packing – Rangpo, Sikkim, India
Junior Operator – Production – Goa, India
Key Information
Details
Job Title
Junior Operator – Production
Location
Goa, India
Job Purpose
Execute production operations in line with safety and GMP requirements
Accountabilities
Operate equipment as per SOPs, suggest process optimizations, ensure cGMP compliance, provide training.
Education Qualification
Diploma in Pharmacy/Mechanical Engineering
Relevant Experience
2 years in manufacturing, preferably pharmaceutical industry
Competencies/Skills
Collaboration, innovation, accountability, agility, domain knowledge, people management
How to Apply
10 Dec 2024
Junior Team Member – QC – Rangpo, Sikkim, India
Key Information
Details
Job Title
Junior Team Member – QC
Location
Rangpo, Sikkim, India
Job Purpose
Prepare, update, and review quality documents to ensure compliance with standards
Accountabilities
Prepare and issue SOPs/specifications, review pharmacopeial updates, execute document harmonization.
Education Qualification
M.Sc./B. Pharma
Relevant Experience
2 years in QC department of a pharmaceutical organization
Competencies/Skills
Collaboration, innovation, accountability, agility, domain knowledge, people management
How to Apply
10 Dec 2024
Junior Operator – Packing
Key Information
Details
Posting Date
24 Sep 2024
Country
India
State
Goa
Location
Goa
Req Id
85727
Division
Manufacturing
Department
Manufacturing
Employment Type
Permanent
Job Purpose
Operate and maintain packing machines to achieve quality product and targeted output with maximum utilization.
Accountabilities
1. Prepare machines for packing operations per production plan. 2. Operate machines efficiently for quality output. 3. Maintain documentation to meet cGMP requirements. 4. Perform operations safely. 5. Train workmen and ensure adherence to cGMP and safety guidelines.
Education Qualification
Diploma in Pharmacy or Engineering
Relevant Work Experience
2 years in packing with knowledge of QMS activities and document handling
Competencies/Skills
Collaboration, Innovation, Accountability, Empathy, Agility, Domain Knowledge, People Management
Job Location
Goa
Shift Hours
Not specified
Quality Assurance (QMS) Production Lead
Key Information
Details
Posting Date
23 Sep 2024
Country
United States
State
Massachusetts
Location
Fall River
Req Id
85031
Job Title
Quality Assurance (QMS) Production Lead
FLSA Classification
Professional, Exempt
Work Location
Fall River, MA
Work Hours
General: 8:30 AM – 5:00 PM (may vary based on business needs)
Reports To
QA Manager
Purpose
Ensure product quality throughout all manufacturing phases per SOPs and guide QA associates.
Scope
Review and approve batch records, manage raw material releases, and handle non-conformance issues.
Education and Experience
Bachelor’s degree in a relevant field; 5+ years in QA within cGMP pharmaceutical manufacturing
Technical Knowledge
Knowledge of pharmaceutical manufacturing machines, compliance audits, SAP system, inhalation products
Professional Competencies
Initiative, team working, problem-solving, fast-paced environment handling, and excellent organizational skills
Work Schedule
May require flexible shifts, including weekends and holidays
Relocation
Negotiable
Conclusion
In conclusion, Cipla provides a wide range of career opportunities for those passionate about advancing healthcare and making a positive impact on people’s lives. With a focus on innovation, quality, and employee development, Cipla offers a dynamic and supportive work environment. For professionals looking to grow their careers while contributing to global health solutions, Cipla represents an excellent platform to achieve both personal and professional success.
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