Rs 12 - 15 lakhs p.a.
...Operating Procedures of overall Quality Control Activities. Protocols related to Method /
Process/ Cleaning/ Analytical Method Validation etc.
To evaluate the Change Control suggestions for overall reviews of non-conformances,
failure investigations, analyzing the...
Rs 3 - 8 lakhs p.a.
...Implementing and ensuring compliance to GQS, HSE and ISO guidelines / standards and maintaining documentation for the same including process validation and qualification.
ISO 14001 and SAP
Adhering to ISO 14001 activities and objectives in Pharma.
Performing all SAP and...
Rs 2 - 4 lakhs p.a.
...for new employee training.
19. Review vendor qualification document.
20. To participate in equipment qualification and process validation programme.
21. To undertake any other job as may be assigned by the Lead quality assurance.
22. Review the deviations and OOS are...
Rs 2 - 6 lakhs p.a.
...Min. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities Technical skills & Competencies / Language
Technical competence.
Leadership skills.
Analytical ability....
Rs 3 - 5 lakhs p.a.
...detailed documentation of QMS(change control, deviation, incident, market complaints, product recall)
VMP: maintain and execution of Validation plan as per schedule
Master index: Prepare and maintain of Master index for SOP, STP, Protocols, MFR, BMR/BPR
Document control...
Rs 2 - 5 lakhs p.a.
...Product transfer protocol and Report • Preparation and Review of Batch Manufacturing Records • Preparation and Review of protocols for validation/verification of product / process • Preparation, Review and certification of validation/verification reports after execution •...
Rs 3 - 8 lakhs p.a.
...technological rules during the production of packaging material as well as during packaging process. Responsibility for corrections and validation of PM within workflow (VistaLink Tool).
Responsible for establishing of new BOM and maintaining existing BOM in SAP or CEP based...
Rs 1.8 - 2.4 lakhs p.a.
...analytical instruments like HPLC, UV, titration, pH meter, Rheometer etc
? Carry out the analytical development, analytical method validation or analytical work
and prepare the reports for bulk, finish and rawmaterials.
? Prepare stability protocols, schedules and...
Rs 4 - 6 lakhs p.a.
...Experience/Technical Skills :
# Should have work experience in ADL Lab /PD Lab
# Should be aware about Method Development and Method Validation
# Should have knowledge of HPLC and GC
# Should have knowledge and Work experience in ADL/R&D /PD Lab for analytical exposure...
Rs 5 - 10 lakhs p.a.
...Development of automation, instrumentation and Electrical for new project / machines.
Technical Documentation and qualification / validation of Process control systems.
Design and engineering in the areas of control systems and instrumentation loop drawings, panel...
Rs 3 - 7 lakhs p.a.
...Chemistry
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements
JOB PURPOSE
Generic
Implement Quality Assurance activities for Pharmaceutical at...
Rs 15 - 30 lakhs p.a.
...safety cultures among all employees.
8. Handling and manpower management, work planning and scheduling as per priorities.
9. Ensure valid safety work permit system in the plant.
10. Audit, analysis and report environmental performance to internal and external team.
11...
Rs 10 - 15 lakhs p.a.
...procedures.
· To analyze critical finished products and new products for Active content and impurity profile.
· Develop/Standardize/validate analytical methods for raw materials and finished products.
· To create secondary reference standards for product analysis and...
Rs 2 - 4 lakhs p.a.
...Function – Should be from formulation background
Area Responsibility – 1. Preparation and review of QMS Document, Execution of process validation, 2. Validation for the tablet / Policy 3. IPQA Instrument Handling . 3 Production Integration ,BMR Review.
QA,QMS,Quality...
Rs 2 - 4 lakhs p.a.
...materials, semi finished product and finished products as per agreed/approved Specification.
# To review and approve analytical reports, validation protocols, calibration reports, environmental monitoring planner and other documents of microbiology laboratory.
# Preparation and...
Rs 1 - 4 lakhs p.a.
..., GC, UV, IR, AAS, FTIR & other Lab Instruments.
Able to perform routine analysis, Method Development in HPLC, GC, also perform Validations.
Aware of Regulatory requirements, Basic knowledge of Documentation Audit
Having an experience 3-5 year in pharma industries...
...namkeen (preferred)
Location: All gujarat
Experience: 1-3 years
Package: CTC + Allowances (Rs.150/day)+ Incentives (As per Co. norms)
Must have’s: Two wheeler with valid Driving license.
Skills: Decent communication skills & Basic Math.
show more
...Conduct analysis of different parameters for process improvements
Ensure timely release of SOP and other documents for new products
Validate system documents like CAPA, RMC and Waste norms
Ensure smooth hand over of process to operations team
Develop KPIs to measure...
Rs 2 - 5 lakhs p.a.
....4 To prepare stock statement on monthly basis.
11.0 Documentation
11.1 Maintain document online as per ISO requirement and validation on regular basis.
11.2 Ensure document filled online and without any deviation.
12.0 Maintain ERP.
12.1 To Prepare...
...Experience
- Education:
- High school or ITI with at last 5 years experience of warehouse/material handling preferred.
- Must hold a valid forklift operator license from a recognized training provider.
- Professional experience:
- Accountability for safe and efficient...
Rs 8 - 12 lakhs p.a.
...contact for all external and internal process concerns from customers and accountable to make the best possible changes in the process and validate the changes
- Define the training of new method, principle, or new machine operation and train to opertaors , supervisors, engineer...
Rs 10 - 15 lakhs p.a.
...Recovery plant, ETP Modifoication and brown field project .
# Handling of All type of agency ( Civil, electrical, Mechanical, all type Validation team, Calibration etc)
# Detailing and control/ Optimization of Budget
# Energy Conservation
#
Project,Project Management...
Rs 10 - 25 lakhs p.a.
...Change control, OOS and Incident
reporting) with QRM
• Ensure timely batch release
• Ensure regulatory compliance, availability of valid Licences and certificates at
the plant
• Ensure availability of customer specific certifications for the plant
ACG Associated...
Rs 3 - 7 lakhs p.a.
# Handling BMR- BPR Preparation
# Filling records as per cGMP
# RM - PM dispensing
# Validation
# Track & Trace
# Coordination with QA/QC
# Maintenance Dept, Maintain product quality and process safety
# Manpower Planning
# Perform other activities allocated...
Rs 5 lakh p.a.
...safety norms and precautions are followed by all production
personal.
To co-ordinate for internal GMP activities
Ensure that Validation protocols and reports are reviewed and approved.
Equipment Handling:
REACTORS (SSR, GLR), MULTIMIL, CENTRIFUGE, NUTCH...
Rs 2 - 12 lakhs p.a.
...Profile HPLC, Analytical Skills
ADL
Roles and Responsibilities Analytical Development lab, HPLC, LCMS, GC
~ Analytical Method Validation as per ICH guideline.
~ Method development.
~ SOP preparation.
~ Stability Studies.
~ Method transfer....
Rs 3 - 5 lakhs p.a.
...analysis time to time
1.3 Finished product analysis and compare to require specification compliance
2. Manage QC lab
2.1 Method validation – Set test methods as pharmacopoeia and GMP requirement.
2.2 Instrument calibration: Prepare calibration Schedule and calibration...
Rs 25 - 40 lakhs p.a.
...Road Map for Collective Bargaining
# Floor Intelligence to champion settlement
# Aligning Committee in off Meetings for LTS
# Validation of Committee members for right representation
# To drive LTS meeting on the basis of consolidation of action plan
# To establish...
Rs 3 - 6 lakhs p.a.
...conference room, visitor room and admin block.
5. To maintain and record of all the flies of plant head office and ensure for its validation.
6. Maintain documents, records rooms.
7. Daily Production tracking.
Position Qualification
Excellent verbal and written communication...
...supervisor/ manager and Mentor junior lab personnel
9.Preparation and review of analytical protocols and reports (Analytical method validation, Method feasibility, Analytical method transfer, etc.).
10.Participate in project meetings and prepare weekly and monthly reports...