SP Accure Labs Walk-In Interview For Engineering & Regulatory Affairs Departments

SP Accure Labs conducting walk-in interview for engineering and regulatory affairs roles was scheduled for Friday, November 29th, 2025. The event took place at their facility in Hyderabad, Telangana, and was aimed at experienced professionals, with formulation experience being mandatory for most roles.

Walk-In Interview Details:

Date:November 29th, 2025

Time: 8:30 AM to 11:00 AM.

Location: Plot No. 12, Biotech Park, Phase II, Lalgadi Malakpet, Shamirpet Mandal, Medchal-Malkajgiri Dist., Telangana State, India.

Target Audience: Experienced professionals (1 to 10+ years) in Engineering and Regulatory Affairs.

Departments and Roles

A.Engineering Department

1.Position: Executive

Experience: 5 to 10 years experience required

Qualification: Diploma/B.Tech qualification.

Skills: HVAC & Water Systems

2.Position: Executive

Experience: 5 to 8 years experience required,

Qualification: Diploma, B.Tech/M.Tech qualification.

Skills:Process Engineering (Mechanical)

3.Position:Executive/Jr. Executive

Experience:3 to 5 years experience required

Qualification: ITI, Diploma/B.Tech qualification.

Skills:Process Instrumentation

B.Regulatory Affairs (RA) Department

1.Position: Officer/ Sr. Executive

Experience:3 to 8 years experience required,

Qualification:M.Sc, B.Pharm, D.Pharma, M.Pharm qualification.

Skills:

Formulation Experience: Preparation, review, and compilation of CTD/eCTD/ACTD dossiers for global markets (EU, Canada, LATAM, GCC, ROW, etc).
Ensure timely submission of new product registration applications, renewals, and variations. Ensure product information (SmPC, labels, artwork, PIL, SPC, IFU) is compliant with, EMA, WHO, ICH, and country-specific guidelines.
Maintain regulatory databases, submission trackers, product registration status and Handling of customer and MOH queries

2.Position:Officer

Experience:1 to 5 years experience required,

Qualification:M.Sc, B.Pharm, D.Pharma, M.Pharm.

Skills:

API Experience: Prepare, review, and compile DMF (Drug Master File), ASMF/CEP, CMC sections of CTD/eCTD for global submissions (EMA, MHRA, TGA, PMDA, WHO, ROW, etc).
Review sections such as S.1-S.7 (General Information, Manufacture, Impurities, Control of DS, Stability, etc.) with current regulatory expectations and ICH guidelines.
Support initial filing, updates, amendments, and annual reports of DMFs/ASMFs/CEPs. Maintain submission trackers, regulatory commitments, and version control of filed documents

Note: The company preferred male candidates and immediate joiners. Outstation applicants could share their CV to jobs@spaccurelabs.com.

SP Accure Labs Walk-In Interview For Engineering & Regulatory Affairs Departments

SP Accure Labs Walk-In Interview For Engineering & Regulatory Affairs Departments