QA

Career @ SavaSeniorCare as a Assistant Manager/Sr. Executive – Quality Assurance

Career @ SavaSeniorCare as a Assistant Manager/Sr. Executive – Quality Assurance

Job Description:
1. Preparation, Review and execution of equipment qualification and validation documents/activities.
2. Preparation and review of apex documents.
3. Training of personnel pertaining to Qualification and validation activities.
4. Preparation of Validation Calendar and Execution support for the same.
5. Documentation cell arrangement for the easy retrieval of documents.
6. To support Validation and Qualification of Equipment as and when requires.
7. QA relevant work as assigned by department head from time to time

Additional Information:
Education : B.Pharm, M.Pharm,M.Sc
Location :  Surendranagar
Indusrty Type: Pharma/ Biotech/Clinical Research
Functional Area: QA
End Date: 2nd Jan, 2017

Forwrd your resume here, shikha.bhati@savaglobal.com

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Opening for General Manager Quality Assurance at CMSS  (Salary: 1,50,000/month)  (Govt Job)

Opening for General Manager Quality Assurance at CMSS (Salary: 1,50,000/month) (Govt Job)

Number of Posts: 1 (One)

Emoluments: 1,50,000/- per month (Consolidated-all inclusive)

Whether Selection Post: On contractual basis for a period not exceeding 5 years or up to reaching the age of 65 years whichever is earlier.

Age limit for direct recruitment: Upto 61 years of age as on the date of advertisement

Main Responsibility
1)To ensure that all procured goods are of the highest quality and meet the specifications as per the purchase order.
2) To ensure that the quality does not deteriorate during storage and distribution.
3) To put in place excellent, quality assurance system through the procurement cycle starting from sourcing till final distribution to ensure the quality of health sector goods.
4)Providing advice on all technical issues relating to procurement of Health Sector Goods.
5)Formulating the generic specifications of health sector goods in consultation with all stakeholders and its up-gradation from time to time.
6) To conduct inspection & testing of contracted goods to ensure supply as per contract specifications.
7) Assessment of vendors, vendor rating and registration of suppliers to maintain directory of suppliers.
8)  Creation of unified standards for inspection of manufactures and suppliers to assess compliance with good manufacturing practices (GMP).
9) Assessment and empanelment of external inspection agencies.
10) To provide inputs to the Supply Chain Management System.
11)    E-procurement relating to quality assurance issues.
12) Other duties as specified or assigned by the Director General /CEO.

Essential Educational Qualification and Experience for direct recruitment
M. Pharma/ M.Sc(Chemistry)/Post Graduate in Bio-Technology

minimum 10 years of experience out of which at least 05 years of experience in inspection, testing & quality assurance of drugs, vaccines and other healthcare products goods for the purpose of procurement thereof, Working Knowledge and experience of Ms Office applications.

Desirable: Proficiency in modern Enterprise Resource Planning (ERP) and E-procurement system is desirable

Probation period: 6-months

Method of recruitment whether direct or by deputation and percentage of the posts to be filled by various methods: On contract basis.

Job requirements: As per attached Annexure

Period of appointment: For retention/continuation, review of performance after every year by the DG & CEO and the Governing Body of the Society. However, services can be terminated by serving two months notice.

Annual increase in salary: 5% subject to satisfactory performance.

Last Date to apply – 5th December, 2016

To apply online, Click here.

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UKA Tarsadia University invites Professors, Associate Professors, Assistant Professors

UKA Tarsadia University invites Professors, Associate Professors, Assistant Professors

Pharmacy: Pharmaceutics, Quality Assurance, Pharmacology, Pharma Analysis, Medicinal Chemistry

Science : Microbiology, Biotechnology, Chemistry, Nano Technology

An outstanding candidate working in industry and with established reputation, and who has made significant contribution to knowledge but not having a Ph D. degree could also be considered for appointment to the post of Associate Professor/Professor on contract basis. Such appointment will be made only sparingly and in extremely deserving cases with the approval of University.

QUALIFICATIONS and EXPERIENCE required for all positions as per UGC/AICTE/INC/COA/IAP/UTU norms.

Salary and benefits will be commensurate with qualification and experience.

Maliba Campus, Gopal Vidyanagar, Bardoli Mahuva Road, Dist: Surat, 394350 Gujarat (India) Email: recruitment@utu.ac.in

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Walk in Interview in QA, Production, QC @ Acme Formulation

Walk in Interview in QA, Production, QC @ Acme Formulation

Quality Control- Officers/Executives
Exposure in Instrumental and chemical analysis i.e. RMPM/FG/Validation/Micro/ Stability and having competency on instruments like HPLC, GC.

Quality Assurance- Officers/Executives
Exposure in IPQA/QMS/ Documentation’Validation,’Qualification with thorough knowledge of cGMP norms.

Production/Packing-Officers/ Technicians
Solid Orals : Experience in Granulation, Compression, Coating,Capsules & Packing (Blister Pack & Cartonator Pack)
Injectable Experience m Vial,’Ampoule Washing Machine, Filling Machine, Lyophilizen’Autoclave & Packing Machine

Interested and eligble candidatess are advised to appear for WALK-IN along wlh updated CV, passport size photograph and salary supporting.

Note: Candidates who are ready to relocate and join us immediately will be preferred.

Timing: 9.30 am to 5.00 pm
Date : 3rd December & 4th December 2016 (Saturday & Sunday)
Venue for Walk in Interview: MEDICO Healthcare, # 501 ,Aditraj Arcade, Near Hetvi Tower, 100, Feet Ring Road, Satellite, Ahmedabad (Gujarat)

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Walk in Interview for QA, QC , Production @ Emcure

Walk in Interview for QA, QC , Production @ Emcure

Quality Control (Micro): Manager/Officers (Injectable)
M.sc (Microbiology) with 2-12 years experience in Microbial analysis, Micro method validation tike BET, MLT, Bioburden & Stenlity. Should have worked in Injectable Plant and having exposure to regulated markets. Excellent communication and people management skills are a must.

Quality Assurance : Officers (Injectable)
M.Sc/B.Pharm with 2-5 years’ experience in Pharmaceutical formulation Industry only for Micro QA reviewer, Chemistry reviewer, Qualification and validation of equipment’s. Analytical data Review. Vendor Audits, Internal Audits, Documentation QMS. hands on expenence in handling HPLCs. GC. IR, OOS, OOT. Investigations, expenence of regulated markets pharmaceutical Injectable formulation plant. Excellent communication and people management skills are must.

Engineering : Manager/Asst. Manager/Executive/Officer
B.E/Dipioma – Electrical/Instrumentation / Mechanical with 2-10 years’ expenence and having exposure to maintenance of plant equipment’s, QMS Documentation, equipment qualification. Should have worked in solid orals & Injectable formulation Plant and having exposure to regulated markets. Excellent communication and people management skills are a must.

Production : Asst. Manager/Officer/Executive
B.Pharm/M.Pharm with 3-12 years’ experience of having exposure in Sterile Injectable Facility in the following sections: Manufacturing, Vial washing. Filling area, Lyophilizer, Autoclave. Tunnel, Isolator. Should have worked in Injectable formulation Plant and having exposure to regulated markets. Excellent communication skills are a must.

WALK-IN INTERVIEWS
Date:
19th & 20th November 2016 at at Ginger Hotel, Vizag 47-10-19,2nd Lane, Dwaraka Nagar, Vlsakhapatnam – 530016, India.
Time : 9.00 am to 5.00 pm

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Senior Executive – QA required @ Pfizer

Senior Executive – QA required @ Pfizer




Roles and Responsibilities: 
• Oversight for implementation of Site Quality procedures for inspecting, testing and controlling raw or packing materials and assessing in-process and finished product to  ensure that all products conform to predetermined Pfizer Quality standards and Compendia Standards and Specifications. Provides or facilitates technical assistance to plant  operations and third party customers.
•   Monitors, audits and approves facilities and manufacturing operations for conformance with established procedures and requirements of the Pfizer and cGMPs. Provides interface between Pfizer and ZHOPL and facilitates investigation of product complaints and to improve customer service/product performance .
•  Ensures maintenance of required records and documents, including tests results, inspections, file samples, supplier performance, product complaints, and product      disposition, local and international regulations.
•  Review and approval of Validation and Qualification protocols and reports as required
•  Reviews and approves the change management requests as required and sits on change control committee.
•  Supports response to field alerts, drug product recalls and returned drug products .
•Reviews and approval of significant non-conformances (Incidents, Deviations, OOS, and  EIR etc.)
• Provides Quality support for Pfizer products and Supports GE (Geographic Expansion)    projects as required.
•     Supports technology transfers from other Pfizer R&D and manufacturing sites.
• Perform GAP assessment for site procedures with the Pfizer Quality standards.
•   Responsible for developing and managing the Supplier Quality to support the Joint venture function.
• Responsible to liase with SMEs and key contacts from Pfizer centre and other Pfizer sites.
• Collaborating with different groups of Joint venture and other Pfizer sites as appropriate   and needed to meet the company and business objectives.
• Responsible for taking sessions related to trainings on the Pfizer process, liasing with cross functional teams on projects etc.

Candidate Profile :
B.Pharm or  M Pharrm in Microbiology / Quality assurance/ Chemistry
The ideal candidate should have excellent written and verbal communication, Strong inter personnel skills, proven ability to deliver outstanding results. Ability to multitask activities to meet the team Goals

Additional Information:
Location: Ahmedabad
Industry Type: Pharma
Last date: 30th November, 2016

To apply online, Click here.

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Opening for Freshers in QC, QA, Production @ Lini Infotech

Opening for Freshers in QC, QA, Production @ Lini Infotech




Job Description :
Qualification; BSC/MSC Frehers
Job Location : Jedcherla
Only Freshers

Candidate Profile :
BSC/MSC Chemistry freshers

Additional Information:
Experience:
Freshers
Qualification: B.Sc, M.Sc
Location: Jedcherla-Telangana
Job Type: Production.QA,QC
Industry Type: Pharma

Email your Resume : careers@liniinfo.com

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Faculty Recruitment at Bharat School of Pharmacy

Faculty Recruitment at Bharat School of Pharmacy




DEAN(ACADEMIC)
Ph.D. in Pharmacy with 10 years teaching expenence should be able to lead the faculty academic activities.

PROF, ASSOC. PROF & ASST. PROF in
PHARM D, HCP/ PHARMACY PRACTICE, PHARM. CHEMISTRY, PHARMACEUTICS, PHARM. ANALYSIS, PHARMACOLOGY, QUALITY ASSURANCE & PHARM BIOTECHNOLOGY
Salary as per revised VIth pay AICTE norms for candidates who completed their PG through GATE / GPAT Scholarships and pursuing or completed Ph.D. For other mentorious candidates salary as per Vth Pay Scale will be extended. Eligibility as per AICTE norms.

If professors unable to attend the interview can send the resumes to secretary@biet.ac.in and can approach the Chairman directly for discussions.
If unable to attend tho intciviow can o mail thoir Resumes to pharmacy@biet.ac.in

Venue: Bharat P.G. College for Women,
Kachiguda, Opp. Tourist Hotel, Hyd.

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Work for QA / QC / Production / Engineering Departments of Hetero Drugs | B.Pharm

Work for QA / QC / Production / Engineering Departments of Hetero Drugs | B.Pharm




Quality Control :
Positions : Jr. Officer – Asst. Manager
Exp. :  2 to 10 years of Experience in QC Dept.

Quality Assurance
Positions : Jr. Officer – Asst. Manager
Exp. :  2 to 12 years of Experience in QA Dept.

Production:
Exp. 2 to 6 years of Experience in Production dept.




Engineering:
Exp. 10 to 25 years of experience in Maintenance department

Interested candidates with experience in Pharma Industry can send profiles to raju.ch@heterodrugs.com

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Novartis looking for Manager Quality Assurance

Novartis looking for Manager Quality Assurance

Job Description
provide the support for External Supply Operations in all quality related matters and to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements and the Novartis Pharma Corporate Quality Manual and Policies.  Implementation of all aspects of the handling and distribution of pharmaceutical products at Novartis India Limited comply with the requirements of the Novartis Pharma Corporate Quality Manual and Policies and meet all relevant cGMP regulatory and legislative requirements. Implement local Quality System and Standard Operating Procedures for all GxP related activities. Provide support to third parties and ensure that they are qualified, achieve a high level of competence and are prepared to carry out their duties in a safe manner. Maintain current knowledge of local and international regulatory and legislative requirements and trends to ensure that technical support on all quality related matters is provided to the third parties. Establish a good working relationship with internal and external customers. Audit and co-ordinate third party activities and ensure that third party manufacture, packaging, labelling, storage and/or distribution of Novartis products is in compliance with Novartis Standards. Handle complaints, recalls, counterfeits and product tampering according to the Novartis Corporate Quality Manual and local written procedures. Provide active QA support to production and third parties during new product launches, site transfers and analytical method transfers. To assist in development of new vendors in co ordination with purchase in accordance with local procedures.

Candidate Profile :
University degree in pharmaceutical / life sciences. Post Graduate degree preferred English & country language 5-6 years

Additional Information:
Experience: 5-6 years
Qualification:  degree in pharmaceutical / life sciences
Industry Type: Pharma/ Healthcare/ Clinical research
Location: Mumbai
Functional Area: Quality
Job ID: 199658BR
Last Date: 25th November, 2016

To apply online, Click here.

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