Page 183 - CW E-Magazine (30-7-2024)

Chemployment Exchange Chemployment Exchange

Scientist – Cell Culture neering or life sciences. Chemical Engi- with the company’s strategic goals and
neering is preferred. objectives.
Lubrizol India Pvt. Ltd. Location: Hyderabad.  Minimum work experience: 2 years of The position is also responsible for
Job summary: We are seeking a dedicated industrial experience with a Ph.D., 6 smooth functioning of certain sections of
Lubrizol India Pvt. Ltd. manufactures and markets fuel & lubricant additives and professional to lead team activities, supervise years with a Master’s, or 9 years with the laboratory, compliance to ESHQ and
speciality performance chemicals for industry. The company requires: lab maintenance, and manage people within a Bachelor’s. regulatory requirements. Overall, the posi-
the upstream process development function  In-depth understanding of cell culture tion plays a critical role in the development
QA Offi cer of Biologics department. This role involves process development for biotherapeu- and implementation of required analytical
ensuring on-time delivery of experiments for tics/biosimilars. methods & techniques and make proactive
Novartis Location: Turbhe, Navi Mumbai. one/two biosimilar molecules, with a focus  Comprehensive data analysis of pro- contributions towards company’s growth
cesses and providing logical conclu-
Role summary: Analytical testing support to internal/external stakeholders by following on drafting and timely closure of technical sions and recommendations. and success.
Novartis, headquartered in Basel, Swit- established QA procedures and guidelines. reports to meet team deliverables.
zerland, is a leading global medicines com-  Knowledge of bioreactor operation in Key responsibilities
batch/fed-batch/perfusion modes.
pany. In India, Novartis has had a signifi cant Key responsibilities Roles & responsibilities Understanding of chemical engineering  Management of analytical method deve-
footprint since 1947, committed to drug  Analytical testing support to production and qualifi cation of materials – raw materials,  Leading and managing the overall scien-  lopment and analysis activities for
development, manufacturing, commercial intermediates, fi nished goods, etc. tifi c, technical, and operational efforts of principles applicable to biotechnology. assigned projects.
and social business services. The company  Prepare, standardise, and maintain all standard solutions for QA. team members.  In-depth understanding of mammalian  Supporting Head-Analytical in smooth
requires:  Maintain instruments and equipment for QA. This includes, but is not limited to, cali-  Overseeing lab operations and equip- cell culture physiology and metabolism functioning of analytical labs.
bration, burette verifi cation, electrode performance checks, preventative maintenance, ment maintenance, actively participating for biosimilar product development.  Ensure that all activities are carried out
Specialist – Quality Operations troubleshooting. in lab meetings, contributing to trouble-  Design of Experiments (DOE) and sta- in accordance with ESHQ guidelines.
 Working in SAP environment. shooting potential causes for experimen- tistical analysis skills using various tools.  Project and KRA related documentation
Job ID: REQ-10015988. tal failures.  Understanding of FDA, EMA, ICH, and
 Takes responsibility regarding safety and analytical data. Accept instruction/training other regulatory bodies’ guidelines for and upkeep of the same.
Division: Operations. from Team leaders as well as supervisors, and QA staff.  Coordinating upstream process deve- biosimilar development.  Technical guidance to the team mem-
lopment for one/two biosimilar projects
 Reporting of nonconformance. bers working on analytical projects.
Business unit: Innovative Medicines.  Additional duties as assigned, etc. within the function.  Plan & ensure availability of all the
 Planning resource requirements, pro- For more details, visit: https://careers. necessary materials or any other aspects
Location: Hyderabad. Key requirements viding guidance to meet project deli- drreddys.com/job/scientist-cell-cul- needed for the successful execution of
 B.Sc./M.Sc. in chemistry from a recognised University. verables, and ensuring project schedules ture-in-hyderabad-jid-856 assigned projects.
Summary: Provide quality services in  Experience in testing of lubricants, additives/oil industry, preferably in MNC environ- are met with quality technical success.
compliance with cGMP requirements and ment.  Contributing to performance reviews (Source: Company website)  Coordinate with the formulation deve-
Novartis Quality Management System as  Experience with analytical instruments e.g., ICP, GC, viscosity, density, XRF, FTIR, auto of team members, identifying deve- lopment managers to ensure timely
analysis of the experiments.
defi ned and agreed between QOP and busi- titrators, wet analytical methods, etc. Minimum 4 years of industry experience prefer- lopmental needs, and maintaining disci- Evonik Coordination with potential vendors
ness partners. Manage quality aspects & ably in SAP environment. pline within the team.  for buying of new equipment & instru-
projects within area of responsibility.  Should be able work in shifts, etc.  Data collation, analysis, and interpreta- Evonik, based in Germany, is a speciality ments, etc.
tion, drawing logical scientifi c conclu-
Major accountabilities For more details, visit: https://jobs.lubrizol.com/job/Turbhe%2C-Navi-Mumbai- sions, and generating technical presen- chemicals company with production plants in Key requirements
 Coordination and management of ana- QA-Offi cer-MH-400703/1158085000/ tations. 26 locations and active in over 100 countries. Minimum of 8-10 years of relevant ex-
lytical method transfers and stability  Drafting scientifi c reports for team deli- The company’s Indian subsidiary requires:  perience in pharmaceutical and specia-
studies. Compilation of data reports. (Source: Company website) verables, maintaining global quality and lity chemicals industry. with a Master’s
 Life-cycle management of analytical risk assessments – nitrosamines, substances/products/medical devices. adhering to regulatory standards. Sr. Associate Manager – Analytical degree/Ph.D. in Pharmacy with pharma
methods, including control of method residual solvents, etc.  GxP knowledge, Basic IT knowledge,  Assuming ownership of specialised pro- Development
performance, pharmacopoeia and health  Implementation of GMP requirements. etc. cess equipment, ensuring compliance ceutical chemistry or pharmaceutical

analysis as a subject of specialisation.
authority compliance and defi nition of Compilation and review of documents with safety standards, and supervising Location: Thane, Maharashtra. Comprehensive understanding of both
method improvements. Handling of (analytical protocols and reports, an- For more details, visit: https://www. safety and lab systems.  established and emerging analytical
deviations, investigation, OOS/OOE/OOT nual performance quality reports, on- novartis.com/in-en/careers/career-  Overseeing inventory updating, trouble- Job ID: R32677. methodologies. Exposure to biologicals
cases as well as changes and complaints. going process verifi cation reports, regis- search/job/details/req-10015988-spe- shooting problems related to equipment,
 Perform statistical data analysis to re- tration documents). cialist-quality-operations and ensuring smooth development work Purpose of the position: The position analysis would be a plus, etc.
port Out of Expectations (OOE), out of  Perform activities of a Quality Con- in the lab, etc. will be a part of RD&I organisation. The For more details, visit: https://evonik.

trends (OOT), etc. trol expert as defi ned by the respective (Source: Company website) employee independently executes the ana- wd3.myworkdayjobs.com/en-US/
 SAP master data management: Mainte- sites, etc. Key requirements lytical development and allied activities for External_Careers/details/Sr-Asso-
nance of master data, creation of Q-info Dr. Reddy’s Labora-  A Ph.D. or Master’s degree (M.Sc. pharmaceutical/nutraceutical products & ciate-Manager--Analytical-Deve-
records and other SAP related activities. Key requirements or M.Tech. or M.E. or M.Pharm.) or technologies. The position supports multiple lopment_R32677?locations=2cfd-
 Validate spreadsheets.  Pharmacy/Science/MBA /Engineering/ tories Ltd. Bachelor’s degree (B.Tech. or B.E. or projects simultaneously and collaborates d81278e601342e10c5b8b500eb17&-
 Collect, transcribe and/or compile data equivalent from a reputed institute. B.Pharm.) in Biology, Chemical Engi- with a team of R&D professionals to ensure locations=2cfdd81278e6011ef-
from various repositories (SAP, LIMS,  Minimum 3 years of experience in Dr. Reddy’s Laboratories Ltd., a leading neering, Microbiology, Biotechnology, effi cient and effective completion of all team 8fa40b9b5004919

external COAs). quality assurance, regulatory or in the multinational pharmaceutical company based Biochemistry, Biochemical Engineer- tasks. The employee also collaborates with
 Author, approve and archive Impurity manufacturing of pharmaceutical drug across global locations, requires: ing or other related disciplines of engi- cross-functional teams to align all projects (Source: Company website)

182 Chemical Weekly July 30, 2024 Chemical Weekly July 30, 2024 183

Contents Index to Advertisers Index to Products Advertised