Bmr Simplification Position
2 weeks ago
Department
- Corporate TS
- Job posted on
- Jan 02, 2025
- Employment type
- P-P7-Probationer-HO Staff
**Job Description: BMR/eBMR Simplification Specialist in Pharmaceutical manufacturing**
**Position Overview**:
**Key Responsibilities**:
- Simplify and optimize BMR/eBMR processes to improve efficiency and compliance.
- Utilize tools such as PFMEA, Value Stream Mapping (VSM), Poka-yoke, Kaizen, and digital interlock to identify and eliminate inefficiencies.
- Identify system touch points and generate solution.
- Working towards reducing line clearance checklist effort to reduce IPQC footprint.
- Collaborate with cross-functional teams to implement process improvements.
- Stake holder management, change management to drive and implement solution.
- Provide training and support to ensure smooth adoption of simplified processes.
- Monitor and evaluate the effectiveness of implemented changes.
**Qualifications**:
- Bachelor's degree in Chemical/Biologics/Mechanical/Production Engineering, Pharmacy, Chemistry, or a related field.
- Minimum of 5-8 years of experience in pharmaceutical manufacturing or quality control.
- Strong knowledge of Good Manufacturing Practices (GMP) and quality assurance principles.
- Excellent communication and interpersonal skills.
- Detail-oriented with a proactive approach to problem-solving.
**Preferred Skills**:
- Experience with Lean Six Sigma or other process improvement methodologies.
- Familiarity with digital manufacturing tools and paperless systems.
- Strong analytical and critical thinking skills.
**Location: Ahmedabad Based Plant
-
Regulatory Affairs Officer
3 days ago
Gota, Ahmedabad, Gujarat, India Noronic Pharmaceutical Pvt Ltd Full time**Company Name - Noronic Pharmaceutical Private Limited** **Position - RA (Regulatory Affairs -"Preferred Experience: Pharmaceutical Industry")** **Responsibilities**: - 1 to 5 Module - CTD/ ACTD - Process Validation (PV) - Stability - PDR - Art work Check - BMR/BPR Preparation - SMPC - Leaflet flit Preparation (Insert) - AMV - CDP Match - Spect COA/MOA -...
-
Regulatory Affairs Executive
1 day ago
Gota, Ahmedabad, Gujarat, India Noronic Pharmaceutical Pvt Ltd Full time**Company Name - Noronic Pharmaceutical Private Limited** **Position - RA (Regulatory Affairs -Preferred Pharmaceutical Industry)** **Responsibilities**: - 1 to 5 Module - CTD/ ACTD - Process Validation (PV) - Stability - PDR - Art work Check - BMR/BPR Preparation - SMPC - Tea flit Preparation (Insert) - AMV - CDP Match - Spect COA/MOA - Finish...
-
Regulatory Affairs Officer
3 days ago
Gota, Ahmedabad, Gujarat, India Noronic Pharmaceutical Pvt Ltd Full time**Company Name - Noronic Pharmaceutical Private Limited** **Position - RA (Regulatory Affairs -"Preferred Experience: Pharmaceutical Industry"** **Responsibilities**: - 1 to 5 Module - CTD/ ACTD - Process Validation (PV) - Stability - PDR - Art work Check - BMR/BPR Preparation - SMPC - Leaflet flit Preparation (Insert) - AMV - CDP Match - Spect COA/MOA -...
-
Production Officer
2 weeks ago
Gota, Ahmedabad, Gujarat, India Noronic Pharmaceutical Pvt Ltd Full time**Company Name -Noronic pharmaceutical Pvt. Ltd** We are looking for detail oriented and proactive to ensure the quality, performance ,reliability of our products. **Position **Key Responsibilities**: - Prepare and set product manufacturing formulas as per production and R&D guidelines. - Prepare and review **Batch Manufacturing Records**(BMR) and...
-
Quality Assurance Officer
5 days ago
Bavla, Ahmedabad, Gujarat, India HCP Wellness Full timeWhatsAppAt HCP Wellness, we believe in delivering trust through every product. As a leading private label manufacturer of cosmetics, personal care, and oral care products, our success is built on a foundation of quality, innovation, sustainability, and customer-first commitment. Our team thrives in a collaborative, compliant, and quality-focused environment...
-
QA/qc Chemist
1 week ago
Ahmedabad, Gujarat, India HCP Wellness Private Limited Full time**Department: Quality Assurance / Quality Control** **Position: Chemist / Sr. Chemist** A leading third party manufacturing company of Cosmetics based at Ahmedabad is looking for **QA/QC Chemist / Sr. Chemist **who can coordinate, manage with all the departments and achieve the highest quality standards and safety of all the products. In this role, you...
-
Quality Assurance(Pharma
7 days ago
Padra, Vadodara, Gujarat, India krishna enterprise Full timeJob Opportunity - *QUALITY ASSURANCE*(Pharma - API Division) Position: QUALITY ASSURANCE OFFICER Location: Vadodara ( Padra ) Requirements:* - Ensure compliance with GMP, GLP, and regulatory guidelines in all QA operations. - Review and approve batch manufacturing records (BMR/BPR) and related documentation. - Handle deviations, change controls, CAPA, and...
-
In-process Quality Assurance
5 days ago
Bavla, Ahmedabad, Gujarat, India HCP Wellness Full timeWhatsAppAt HCP Wellness, we are committed to delivering safe, effective, and high-quality cosmetic and personal care products. As a trusted private label partner, we uphold the values of integrity, innovation, compliance, and continuous improvement in every aspect of our operations. We foster a work culture where quality, customer focus, and collaboration...
-
QA Documentation
5 days ago
Savli, Vadodara, Gujarat, India krishna enterprise Full time**Position Title: QA Documentation** **Location**: Vadodara (Savli) **Department**: QA **Qualification** : M.sc in Organic chemistry **Experience** : Up to 5 Year **Job Summary**: Responsible for managing, preparing, reviewing, and controlling quality-related documentation to ensure compliance with regulatory requirements, company policies, and industry...
-
QA Executive
1 day ago
Nandesari Ind. Estate, Vadodara, Gujarat, India Easy HR Solution Full timeJob description: - **Position: QA Executive**: - **Experience: 2 to 5 Years**: - **Qualification: B.Sc / M.Sc**: - **Industry: API / Pharma Manufacturing**: - **Location: Nandesari, Vadodara** **Roles & Responsibilities**: - Preparation, review, issuance, and archival of GMP documents such as SOPs, BMRs, BPRs, protocols, and logbooks. - Ensure...