Chemveda Life Sciences is a mid-sized, rapid-growing solution provider to the pharmaceutical, biotech, academia, and agrochemical industries. As a contract research partner Chemveda is boosting its value creation along and beyond the drug discovery & development continuum with a strong focus on churning out cost and timeline efficiencies for its global clientele.
Chemveda harnesses its command over science and technology to deliver full suite Chemistry support spanning from lab scale synthesis, till industrial Process R&D, and large-scale custom development of drug substances, key intermediates, and starting materials. Lately, we have been invested in developing in-house capabilities on the most sought-after scientific platforms to answer the existing and evolving challenges in the field of basic and applied research.
Founded and headquartered in 2008 in Hyderabad, Chemveda is over 350 employees strong with a technology-based division of teams. We have our US presence through our office in San Diego and also a team of same-time zone project managers & consultants deployed across the major biotech hubs of US, Europe, and Asia.
Chemveda witnessed steady growth until 2016, which marked as a turning point with a change of hands, and a more conducive decision making and cash-flow. The first step soon after this change was to strengthen the scientific core which started with Prof. Nicolaou being inducted as a mentor which has now grown to the likes of Prof. Phil S Baran, Prof. Jin Quan Yu, Prof. Scott Snyder, Prof. David Yu-Kai Chen, and Prof. David Sarlah. This proved to be the most instrumental step in creating a team of self-sustained thought leaders and support system and is still continuing to be so.
Being solely a service provider all our offerings are based on a strong foundation for safeguarding the clients IP and zero-conflict mix of investors, none of whom come from the allied industry.
Strong focus on people has always been a core to our expansion and we have empowered them with the latest infrastructure, systems and processes, and desired equipment ratio which is either on par or better than the industry standard. We have completed two stages of expansion and set for third stage at this moment.
As we achieve the milestones of growth we wish to grow not only in terms of our scientific capabilities and human talent, but also by generating qualitative as well as quantitative value for our clients as well as shareholders.
DATE AND TIME:
Date: 27th June 2025 (Friday)
Time: 09:00 AM to 12.00 PM
VENUE:
Plot No. B-11/1,,,IDA Uppal,Hyderabad, Telangana, India (View on map)
Contact – Sai Vardhan ( 6309995773 )
Interested candidates can attend walk-in drive or share their profiles to saivardhan.kothuri@chemvedals.com
Job Description:
Position Name: Fresher/Executive
Experience – 0 -5 years
Qualification – M.Sc Chemistry /M.Pharma
Designation – Executive
Job Responsibilities :-
1. Involves in daily QA activities for SOP compliance.
2. Equipment and Software qualifications Review of USR & SRS, Review of IQ, OQ, PQ document inhouse softwares and maintenance of Equipment and software related back up coordination with other departments.
3. Preparation of refresh and QMS Training presentation and circulating training links to all employees based on training schedules and follow ups.
4. Review of Risk assessments related to change control, CAPA, Deviation, OOS, OOT.
5. Review of Analyst Qualifications and review of Analytical LNBs.
6. Review of Vendor Questionnaires and Review of Vendor qualification documents and checking external facility and vendor audits with respect to raw materials and finished products.
7. Review of new GMP projects with regard to regulatory and client compliance aspects, Scrutiny of GMP facilities and Review of GMP Certifications & all requirements applicable to the projects.
8. Review of SOPs, Specifications, Method of Analysis and Analytical test data sheet.
9. Review of Method transfer protocols and reports, Validation protocols and reports, Forced degradation data and Review of quality impacting incidents, OOS and Data corrections.
10. Lab rounds and Compliance verification and Qualification of GMP Contract Manufacturing Facilities (CMO).
a. Circulation of Non-compliances
b. Circulation of Non-Compliance reports to CMO
11. Circulating agenda for Internal Audits and Management review meetings, Reporting & Circulation of Non-Compliances and Suggestion of appropriate CAPAs.
12. Functional Objectives: Follow-up & review of the objectives action plan and Data collection & compilation.
13. Review of weekly and monthly reports and collecting data.
14. Monitoring of QMS activities as per ISO & Client requirements.
15. Document issuance, retrieval and archival, document control.
16. During the audits, to coordinate with the with the auditors to show and explain the documentation of quality systems & procedures.
17. Preparation quality system procedures and quality manual.
18. To prepare audit compliance reports or responses and to ensuring the successful closure of audit cycle.
Education:
MS/M.Sc(Science) in Organic Chemistry, Chemistry, M.Pharma in Pharmacy
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