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Asst. Manager QC :
Experience: 6-10 Years in UFDA Approved Reputed
Pharmaceuticals (Bulk drug) company
Qualifications: M.Sc. Analytical Chemistry/M.Sc.
Organic Chemistry.
Total Responsibility of overall functioning of the Quality
Control Laboratory in accordance with cGLP and principles
of GMP including Instruments.
Having exposure of new Laboratory set up, USFDA, MHRA approval,
Train and develop all QC staff on cGLP, analytical techniques
and their evaluation on periodical basis.
Hands on Experience of analytical Instruments and Validation
of Equipments/Instruments, method validation as per ICH Guideline.
Organize the analysis of all stability samples, as per specified
schedule.
To ensure the quality of Potable water, Purified water and
DM water and provide the feedback on necessary action on bio-burden.
Co-ordinate with other Depts for routine activity and QC Dept.
Having regulatory audit exposure including handling of Deviations,
Change controls and OOS.
QC officer /Analyst :
Experience:
Min. 2 Years in USFDA/MHRA Approved Reputed Pharmaceuticals
(Bulk drug) company.
Qualifications: M.Sc. Analytical Chemistry.
Operation and calibration of HPLC, GC , FTIR Instruments
analytical instruments. Accurate and timely documentation
of all analysis including raw data, checking of all data and
proper storage of data and timely reporting of Results.
Proper standardization of volumetric solutions, preparation
of reagents and its documentation.
Sampling, storage & control of Raw materials/Finished
product retention
3.0 - SHE officer
Safety Health and Environment :
Experience: Min. 6 Years in Reputed Organisation
preferably Pharmaceuticals company.
Qualifications: M.Sc. Environment + Safety
Diploma
Total Responsibility of overall functioning of the EHS as
per Factory Act. i.e implementation of EHS Systems such as
Accident Investigation/Reporting, Safety Work Permits and
training for all level employees.
Evaluation and Implementation of the EHS legal compliance,
documentation as per EHS legal compliance and GMP requirement.
Environmental monitoring for air, water, soil and waste. and
responsible for fire extinguishers, fire hydrant system, emergency
fire and safety appliances and equipments.
To established ETP and Safety systems for smooth running of
factory.
Self correspondence, assisting to managing director in his
day to day activities, , all secretarial work like typing
of correspondence, arranging meeting and sending agenda and
notice of the same to concern persons, Handling travel desk
- domestic and international, hotel booking and arrangement
of transportation for visitors
Asst. Manager QC :
Experience: 6-10 Years in UFDA Approved Reputed
Pharmaceuticals (Bulk drug) company
Qualifications: M.Sc. Analytical Chemistry/M.Sc.
Organic Chemistry.
Total Responsibility of overall functioning of the Quality
Control Laboratory in accordance with cGLP and principles
of GMP including Instruments.
Having exposure of new Laboratory set up, USFDA,MHRA approval,
Train and develop all QC staff on cGLP, analytical techniques
and their evaluation on periodical basis.
Hands on Experience of analytical Instruments and Validation
of Equipments/Instruments, method validation as per ICH Guideline.
Organize the analysis of all stability samples, as per specified
schedule.
To ensure the quality of Potable water, Purified water and
DM water and provide the feedback on necessary action on bio-burden.
Co-ordinate with other Depts for routine activity and QC Dept.
Having regulatory audit exposure including handling of Deviations,
Change controls and OOS.
Microbiologist (Executive) :
Experience: Min. 4 Years in USFDA/MHRA Approved
Reputed Pharmaceuticals (Bulk drug) company.
Qualifications: M.Sc. Microbiology with FDA
approval.
Total Responsibility of overall functioning of the Microbiology
Laboratory in accordance with cGLP and principles of GMP including
Instruments/Equipments.
Having exposure of new Laboratory set up
To ensure the quality of Potable water, Purified water and
DM water and provide the feedback on necessary action on bio-burden.
Having hands on experience of Endotoxine testing, Environmental
monitoring and Bio burden test.
Practical exposure of Microbiology Equipment/Instruments Qualification/Validation.
QC officer /Analyst :
Experience: Min. 2 Years in USFDA/MHRA Approved
Reputed Pharmaceuticals (Bulk drug) company.
Qualifications: M.Sc. Analytical Chemistry.
Operation and calibration of HPLC, GC , FTIR Instruments analytical
instruments. Accurate and timely documentation of all analysis
including raw data, checking of all data and proper storage
of data and timely reporting of Results.
Proper standardization of volumetric solutions, preparation
of reagents and its documentation.
Sampling, storage & control of Raw materials/Finished
product retention
Executive : Safety Health and Environment :
Experience: Min. 6 Years in Reputed Organisation
preferably Pharmaceuticals company.
Qualifications: M.Sc. Environment + Safety Diploma
Total Responsibility of overall functioning of the EHS as
per Factory Act. i.e implementation of EHS Systems such as
Accident Investigation/Reporting, Safety Work Permits and
training for all level employees.
Evaluation and Implementation of the EHS legal compliance,
documentation as per EHS legal compliance and GMP requirement.
Environmental monitoring for air, water, soil and waste. and
responsible for fire extinguishers, fire hydrant system, emergency
fire and safety appliances and equipments.
To established ETP and Safety systems for smooth running of
factory.
QA Dept :
Senior manager Post 5 Years Experiences Must have faced any
international audit. Fluent in English & full knowledge
of latest computer software’s, QA Executives
Min 2 years Experience in Documentation must be aware of WHO
GMP guidelines for Bulk Drug API Facilities
QC Dept :
Senior manager Post 5 Years Experiences Must have faced any
international audit. Fluent in English & full knowledge
of latest computer software’s, QC Executives
2-3 years experience in Raw material Finished goods analysis,
Basic instruments knowledge, Basic, Computer knowledge.
Production Dept :
Qualifications : BSc, Msc, B.E / Diploma
( chemical ) :- Minimum 3 years experience in working in Production
Dept of API company, proficient in English, exposure to documentation
as per Schedule M & WHO GMP requirements, knowledge in
process flow , reactors Typical to bulk drug industry must.
Location: Tarapur, Ambernath, Badlapur &
Dombivili.
Analytical Development Manager :
| Experience : |
10-12 years / 7-8 years |
| Qualification : |
M. Sc . / Ph. D |
| Required Profile : |
 |
Analytical method development for
finished pharmaceutical formulations, |
|
Analytical method validations, |
|
Instrument qualifications, stability study and
necessary documentations. |
|
Well versed with European guidelines and other
international guidelines for analytical method development
and their validation. |
|
Preference Person who as worked as manager or
group leader in a well-known pharmaceutical company. |
|
Officer / Executive :
Regulatory Affairs
Msc Org/Analytical/ Dip in Pharma Mgmt. with at least 1-3
yrs of Exp. in a API manufacturing unit which is FDA approved.
Sound knowledge of using different modes of communication
is a must.
Should be fluent in English language i.e. oral and written.
Shall be reporting to Mgr – Regulatory Affairs.
Officer / Executive :
Research & Development - 2 posts
MSc Organic with at least 2 -4 yrs of Exp in R&D of API
mfg unit. Should have a sound knowledge of working on multi
step organic synthesis. Carrying out different reactions as
assigned by the Group leaders.
Technical Associate :
|
Bsc or Diploma Chemical Engg |
|
Experience from Fresher to 5 yrs in Bulk Drugs & for sterile
also the same. |
|
Knowledge of English is must [Not fluent but at least good] |
|
Need people for API production & Sterile API production |
QA Manager :
Job Profile: Responsible for quality compliance
of all activities of API manufacturing unit. Conversant with
ICH and cGMP guidelines, validation, documentation and audit
requirements of API manufacturing unit.
Qualification: B. Pharm, Msc, BSc (Chemistry)
Experience: 8-10 years.
M Sc / B Sc. Chemist : (Male or female)
Required at Ambernath, Dombivili, Turbhe, Badlapur, Boiser
& Mahad.
Salary: Negotiable
Fresher or Any Year Experience in Production, R&D,
QA & QC dept from Bulk Drugs - API industries.
Chemical Engineer for Production, Project & Process
dept.
Degree/ Diploma fresher or experience
Salary depends on experience and knowledge
Required at Ambernath, Dombivili, Turbhe, Badlapur, Boiser
& Mahad.
Apply now
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