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QC officer/executive in Lupin limited


» Job Posted on Feb 27, 2017

Walk-in for Macleods Pharmaceuticals Ltd on 5th March 2017 at 09:30 AM


» Job Posted on Feb 24, 2017

Walk-in for Sun Pharma on 26 Feb 2017 at 09:30 AM



Job Title*:Walk-in
Company Name*:Sun Pharma
Venue*:Hotel Clarks International
Pinjore-Baddi-Nalagarh Road
Baddi, Solan, Himachal Pradesh 160071
India
Contact Person*:HR
Job Department*:Quality Assurance, Quality Control, Production
Job Details*:OFFICER / SR. OFFICER / EXECUTIVE
Candidates having educational qualifications of B.Sc/ M.Sc/ B.Pharm/ M.Pharm with required subject of specialization (as mentioned below) with more than 2 years of experience in-
PRODUCTION & PACKING (OSD, Parenteral/ Injectables): Location: Mohali (OSD), Gujarat (Parenteral/ Inj)
B.Pharm having experience in manufacturing (Granulation/ Compression/ Capsulation) or Packing of Solid Orals, Parenterals & Injectables. Knowledge / Experience to Compliance processes /guidelines desirable.
QUALITY CONTROL:
Quality Control (OSD/ Parenteral/ API): Location: Gujarat only
Specialization in Chemistry / Organic Chemistry /Analytical Chemistry with experience in Calibration / Analysis / Analytical method validation in QC/ PM / Stability labs. Working knowledge of instruments like HPLC/ GC/ Dissolution/ UV Spectrophotometer, etc. is essential Documentation & New Product Launch exposure are desired.
QUALITY ASSURANCE:
Quality Assurance (Parenteral/ Injectable): Location: Gujarat only
Experience of more than 5 years in IPQA/ QA Microbiology/ QA Documentation/ Quality Engg /Cleaning Validation / Compliance /QMS / Batch Release / Validation etc in Parentage / Injectables dosage forms.
Regulatory Exposure*:Not Required
Experience:2-6 years
Interview Date*:26 Feb 2017 at 09:30 AM


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» Job Posted on

QC Chemist in Ishita Drugs & Industries Ltd.


Company Name*:Ishita Drugs & Industries Ltd.
Venue*:401, 3rd Eye II,
Opp. Parimal Garden, C.G. Road,
Ahmedabad, Gujarat 380006
India
Contact Person*:Jayesh Dhorda
Phone:9228016100
Email Address*:ishitadrugs@vsnl.net
Job Department*:Quality Control
Job Title*:QC Chemist
Qualification*:M.Pharma, B.Pharma, M.Sc, B.Sc.
Required in*:Formulation Unit
Job Details*:Job involves QC functions in a Pharma industry, Testing, and Analysis of various Raw Materials, Finished Drugs, etc. The job requires coordination with production, Stores, and Full knowledge of documentation as per cGMP. experience in similar industry maintaining cGMP conditions, and proper records maintenance essential.
Knowledge of Instrumental analysis on GC, HPLC also required

Desired Candidate Profile
The suitable candidate must have relevant QC experience working in a Pharma QC lab with a proven track record. The person must have very sharp analytical faculties and must possess robust knowledge of chemistry and analytical techniques. He must be familiar with, all QC testing equipment, GC, HPLC etc. Apart from this, a thorough knowledge of cGMP record keeping and GMP implementation is a necessity. Must have demonstrated capability to take independent decisions relating to QC lab work
Regulatory Exposure*:Required
Experience*:3-6 Years
Vacancies *:2
Last Date*:15/03/2017
Additional Details:Interested candidates can send their resume to above email address to apply for this job.
Note:Please send your resume to above email address to apply for this job.


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» Job Posted on

Walk-in for Sun Pharma @Halol, Mohali, Panoli on 19th Feb 2017 at 09:30 AM



Job Title*:Walk-in
Company Name*:Sun Pharma @Halol, Mohali, Panoli
Venue*:Hotel The Deccan Royaale
573/2, J.M Road, Shivaji Nagar
Pune, Maharashtra
India
Contact Person*:HR
Job Department*:Quality Assurance, Quality Control, Microbiology, Production
Job Details*:OFFICER/ SR. OFFICER / EXECUTIVE
Candidates having educational qualifications of B.Sc/ M.Sc/ B.Pharm/ M.Pharm with required subject of specialization (as mentioned below) with more than 2 years of experience in-
QUALITY CONTROL: (OSD/ Parenteral/ API)
Specialisation in Chemistry/ Organic Chemistry/ Analytical Chemistry with experience in Calibration/ Analysts/ Analytical method validation in QC/ PM / Stability labs. Working knowledge of instruments like HPLC/ GC/ Dissolution / UV Spectrophotometer etc. is essential. Documentation & New Product Launch exposure are desired.

QUALITY ASSURANCE: (Parenteral and Injectable)
Experience in IPQA/ QA Microbiology/ QA Documentation/ Quality Engg/ CSV/ Compliance/ QMS/ Batch Release/ Validation etc in Parenteral/ Injectables dosage forms.

PRODUCTION (Formulation)
B Pharm having experience in manufacturing (Granulation/ Compression/ Capsulation) of Solid Orals, Parenterals & injectables. Knowledge/ Experience to Compliance Processes/guidelines desirable.

PRODUCTION (API)
Diploma/ B.E Chemical Engineering or B.Sc / M.Sc in chemistry having experience in production in API/ Chemical manufacturing plants.

TECHNICIAN (Formulation)
ITI / Diploma in Pharmacy/ HSC with experience more than 2 years
Regulatory Exposure*:Not Required
Experience:2+ years
Interview Date*:19th Feb 2017 at 09:30 AM


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» Job Posted on Feb 17, 2017

Walk-in for Hetero Drugs @Jadcherla on 18-19 Feb 2017 at 10:00 AM


» Job Posted on Feb 16, 2017

Walk-in for Zydus Cadila @Ahmedabad on 19th Feb, 2017 at 09:30 AM



Job Title*:Walk-in
Company Name*:Zydus Cadila @Ahmedabad
Venue*:The Metropolitan Hotel
Bangla Sahib Road
New Delhi, New Delhi 110001
India
Contact Person*:HR
Phone:01142500200
Job Department*:Quality Control, Microbiology, Production, Engineering
Job Details*:Vaccine Manufacturing : M.Sc. (Microbiology/ Biotech) with 1 to 8 years of hands-on experience in handling of specific pathogen-free eggs (SPF), embryo isolation, complete MEM preparation, initiation of primary cell culture. cell count, sampling of material for sterility testing during production process & scale up of production process.

Quality Control (OSD/ Injectable) : B.Sc/ B.Pharm/ M.Sc. with 2 to 12 years of hands-on experience in HPLC. GC, dissolution apparatus and UV-visible spectrometer. Should also have knowledge of wet analysis, stability studies for oral solid dosage or injectable forms.

Engineering : B.E / B.Tech (Mechanical/ Instrumentation) with 4 to 10 years of pharmaceutical (formulation manufacturing) plant maintenance experience in PLC/ SCADA/ HMI related work, calibration & validation of instruments / equipment. Exposure to QMS documentation, equipment installation qualification in an OSD plant will be an added advantage.
Regulatory Exposure*:Not Required
Interview Date*:19th Feb, 2017 at 09:30 AM
Additional Details:For all the positions, it is essential for candidates to have exposure to regulatory requirements of documentation and cGMP / GLP. Those with experience in SAP environment shall be preferred.


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» Job Posted on

Sr. Manager Production / Deputy Plant Manager in Blue Cross Laboratories Pvt Ltd.


» Job Posted on Feb 13, 2017

Sr. Executive/ Executive in Alembic Pharmaceuticals Limited


» Job Posted on Feb 10, 2017

Walk-in for Zydus Cadila @Sikkim on 12th Feb 2017 at 9.00 AM



Job Title*:Walk-in
Company Name*:Zydus Cadila @Sikkim
Venue*:Legend Sarovar Portico,
Industrial Town of Baddi,
District Solan, Himachal Pradesh 173205
India
Contact Person*:HR
Job Department*:Quality Assurance, Quality Control, Production
Job Details*:We are recruiting for our manufacturing plant at Sikkim (QC / QA / Manufacturing / Packing) WALK-IN INTERVIEW at Baddi, Sunday, 12th February 2017 9.00 a.m. to 5.00 p.m

Quality Control-Tablet/Capsule/MDI/Topical
Qualification: B.Sc./ B.Pharm/ M.Sc. with 3 to 10 years hands-on experience of handling HPLC, GC, dissolution apparatus and UV. Should also have knowledge of weight analysis and stability studies for OSD, MDI and external preparations.

Quality Assurance - Tablet/ Capsule/ MDI/ Topical
Qualification: M.Sc./ B.Pharm/ M.Pharm with 3 to 10 years of relevant experience in IPQA activities/ calibration & qualifications/ Quality Management System in OSD, MDI and external preparation.

Manufacturing - Tablet/ Capsule/ MDI/ Topical
Qualification: ITI / D.Pharm/ B.Pharm/ M.Pharm with 3 to 10 years of hands-on experience in supervision & operations, monitoring & related documents for OSD. MDI and external preparations.

Packing - Tablet/ Capsule/ MDI/ Topical
Qualification: ITI/ D. Pharm/ B.Pharm/ M.Pharm with 3 to 10 years of hands-on experience in supervision & operations, monitoring & related documents for OSD. MDI and external preparations.
Regulatory Exposure*:Not Required
Experience:3-10 years
Interview Date*:12th February 2017 at 9.00 AM


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» Job Posted on

Walk-in for USV Private Limited on 12th Feb 2017 at 10:00 AM


» Job Posted on

Walk-in for Sun Pharma on 5th Feb 2017 at 09:30 AM


» Job Posted on Feb 4, 2017

Walk-in for Macleods Pharmaceuticals Ltd on 29 January 2017 at 09:30 AM


» Job Posted on Jan 27, 2017

Walk-in for Sun Pharma @Mohali on 29 January 2017 at 09:00 AM


» Job Posted on

HR Manager in GMS Pharmaceuticals pvt ltd


» Job Posted on Jan 24, 2017

Production Executive, Stores Executive , Production officer in KEVYS LABS


» Job Posted on

Officer, Executive in Acme Formulation Pvt Ltd.


» Job Posted on Jan 20, 2017

Walk-in for Torrent Pharmaceuticals Ltd on 22 January 2017 at 10:00 AM


» Job Posted on

Walk-in for Cipla Ltd. on 22 January 2017 at 10:00 AM


» Job Posted on

Engineering Head in Jackson Laboratories Pvt Ltd


» Job Posted on Jan 19, 2017

Stores Manager in Jackson Laboratories Pvt Ltd


» Job Posted on

Production Officer SVP in Jackson Laboratories Pvt Ltd


» Job Posted on

Microbiology Manager in Jackson Laboratories Pvt Ltd


» Job Posted on

QC Manager, QC Executive in Jackson Labs Pvt Ltd


» Job Posted on

Walk-in for Emcure Pharmaceuticals Limited on 21-22 January 2017 at 09:00 AM



Job Title*:Walk-in
Company Name*:Emcure Pharmaceuticals Limited
Venue*:Hotel Pearls, Venture by Motiwala Group
Ground Floor, Motiwala Trade Centre, New Samarth Nagar
Aurangabad, Maharashtra 431001
India
Contact Person*:HR
Job Department*:Quality Assurance, Quality Control, Microbiology, Production, Engineering
Job Details*:Quality Control (Microbiology) - Officer (Injectable)
Qualification: M.Sc Microbiology
Job Profile: 2-5 years experience in microbial analysis, microbial method validation, BET, sterility and experience in injectable plant, exposure to regulatory market.

Quality Control - Officer/ Executive (Injectable)
Qualification: M.Sc/ B.Pharma
Job Profile: 2-6 years experience in quality control laboratory in handling of HPLC, GC, IR etc instruments and experience in laboratory documentation as qualification, lab investigation, deviation etc.

Quality Assurance - Officer (Injectable)
Qualification: M.Sc/ B.Pharma
Job Profile: 2-5 years experience in pharmaceutical formulation for reviewing micro and qc analytical data and qualification and validation of instruments, vendor audit, internal audit etc.

Engineering - Officer/ Executive/ Ast. Manager/ Manager (Injectable $ oral solids)
Qualification: BE/ Diploma (Electrical/ Mechanical/ Instrumentation)
Job Profile: 2-10 years experience in instrument maintenance, equipment qualification, documentation in solid oral and injectable formulation plant.

Production - Officer/ Executive (Injectable)
Qualification: B.Pharma/ M.Pharma
Job Profile: 3-6 years experience in sterile injectable manufacturing, vial washing, filling area, autoclave, tunnel, isolator and other related areas.
Regulatory Exposure*:Not Required
Experience:2-10 years
Interview Date*:21-22 January 2017 at 09:00 AM


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» Job Posted on Jan 18, 2017

Sr. Manager QA / QC (Pharma API/ Bulk Drug), Raigad in Aspiring Solutions


Company Name*:Aspiring Solutions
Venue*:Mahad

Raigad, Maharashtra 402301
India
Contact Person*:Reema Nambiar
Phone:09768813790
Email Address*:aspsol.recruitments@gmail.com
Job Department*:Quality Assurance
Job Title*:Sr. Manager QA / QC (Pharma API/ Bulk Drug), Raigad
Qualification*:MSc Chemistry
Required in*:API Unit
Job Details*:We are urgently hiring for Sr. Manager QA-QC for a reputed API/ Bulk Drug co. for their plant located at Mahad (Raigad). Please find the details below:

Position: Chief Manager QA/QC & RA

Department: QA/QC & RA

Location: Mahad, Maharashtra

Reporting Functionally to MD/CEO and Administratively to Head-Operations

Qualification & Experience: M.Sc. with minimum 18 to 25 years experience. Should have faced regulatory audits such as USFDA, WHO-GMP, EDQM/COS, KFDA, etc. and vendor audit, customer audit, etc.

Age: 40-48 years

Job responsibilities
· To ensure efficient and effective management of Regulatory Affairs, QA & QC functions
· Monitor regulatory environment and ensure that manufacturing practices comply with the regulatory requirements
· Ensure strict compliance to cGMP/GLP guidelines in all areas of QC lab
· Prepare documentation packages for submission to various overseas regulatory agencies
· Evaluate levels of in-house regulatory compliance and prepare answers to queries from regulatory authorities
· Encourage quality improvement programs and reduce costs of quality
· Define goals for validation and decide on the scope of all validation exercises related to products, processes and facilities
· Ensure timely approval of material by quality control and also to enable timely dispatch of finished products in accordance with statutory rules and regulations and customer requirement
· Provide guidance to Training Managers and approve all cGMP/GLP training programs for technical functions
· To review and approve all cGMP related documents
· Conduct self-inspection audits as lead auditor and ensure the compliance to cGMP requirements
· To approve or reject all finished products
· To conduct vendor audits & approval of new vendors
· To review stability study data and establish expiry or retest date
· Implement corrective measures on the basis of quality audits, out of specification, deviation data and market complaint analysis
· To review and approve of documents with respect to change controls, market complaints, deviations, OOS, reprocess, OOT, returns and annual product quality review
· Approving all procedures, specifications, BPRs, laboratory control records before release
· Should have Regulatory Affairs experience

CTC range: Upto 25 lacs per annum

Industry preference: Pharma / Bulk Drugs / API

Candidates preferred from Chiplun, Roha, Mahad, Patalgana MIDC, Taloja Industrial Area


If the position interests you, please email your cv at aspsol.recruitments@gmail.com with details on current CTC, expected CTC and notice period
Regulatory Exposure*:Required
Audit Experience:USFDA, MHRA, TGA, MCC, EMA, UNCST, ANVISA, WHO, HC
Experience*:15+ Years
Vacancies *:1
Salary Per Annum:25 lacs per annum
Last Date*:28/02/2017
Additional Details:Accommodation will be provided
Note:Please send your resume to above email address to apply this job.


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» Job Posted on Jan 16, 2017