Strava Hiring QA, QC, Production & Engineering

BPharm QA QC Production Jobs Ahmedabad | Strava

B.Sc, M.Sc, B.Pharm pharma vacancies at Strava Healthcare Ahmedabad for QA, QC, Production & Engineering (1–5 yrs).

Strava Healthcare Pvt. Ltd. is expanding its pharmaceutical manufacturing operations at Bavla, Ahmedabad, and is inviting qualified professionals to join its Quality Assurance, Quality Control, Production, and Engineering teams. This hiring drive is ideal for candidates looking for regulated pharma plant jobs in Gujarat with strong exposure to GMP, QMS, and tablet/capsule manufacturing systems.

If you are actively searching for B.Pharm jobs in Ahmedabad, QA officer vacancies in pharmaceutical companies, QC microbiology roles, tablet manufacturing production jobs, or pharma engineering QMS openings in Gujarat, this opportunity offers structured growth within a compliance-driven pharmaceutical environment.

---

Company Overview

Strava Healthcare Pvt. Ltd., located at Bavla-Sanand Road, Ahmedabad, operates as a growing pharmaceutical manufacturing organization focused on quality-driven production systems. The company follows Good Manufacturing Practices (GMP), Quality Management Systems (QMS), and regulatory documentation standards required in modern pharmaceutical manufacturing facilities.

With increasing demand in domestic and semi-regulated markets, Strava Healthcare continues strengthening its Quality Assurance, Quality Control, Production, and Engineering capabilities. The company emphasizes documentation discipline, deviation control, validation compliance, and batch traceability to ensure product safety and regulatory adherence.

Professionals joining Strava gain exposure to pharmaceutical compliance systems, audit preparation, documentation review processes, and tablet/capsule manufacturing operations aligned with industry standards.

---

Job Role & Responsibilities

Quality Assurance (QA)

Position: Officer to Sr. Executive
Experience: 1–5 Years
Qualification: B.Sc, M.Sc, B.Pharm

Key Responsibilities:

• Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
• Handle deviation, CAPA, change control, and incident documentation.
• Support internal audits and regulatory inspections.
• Ensure adherence to SOPs and cGMP compliance across departments.
• Monitor process validation and cleaning validation documentation.
• Conduct line clearance and in-process quality checks.

QA professionals play a critical role in maintaining pharmaceutical data integrity, regulatory compliance, and product quality standards.

---

Quality Control (QC – Reviewer)

Position: Officer to Sr. Executive
Experience: 1–5 Years
Qualification: B.Sc, M.Sc, B.Pharm

Key Responsibilities:

• Review analytical reports and raw data for accuracy and compliance.
• Ensure laboratory documentation meets GLP standards.
• Monitor instrument calibration and verification schedules.
• Support stability studies and finished product testing.
• Maintain compliance with regulatory and internal quality systems.

QC reviewers ensure that analytical testing data remains audit-ready and compliant with pharmaceutical quality guidelines.

---

Quality Control – Microbiology

Position: Officer to Sr. Executive
Experience: 1–5 Years
Qualification: B.Sc, M.Sc, B.Pharm

Key Responsibilities:

• Perform environmental monitoring and microbiological testing.
• Conduct microbial limit tests and water analysis.
• Maintain sterility testing documentation.
• Ensure laboratory compliance with GMP and GLP practices.
• Support audit preparation and documentation review.

Microbiology roles are essential for maintaining contamination control and pharmaceutical product safety.

---

Production – Tablet / Capsule Manufacturing

Position: Officer to Sr. Executive
Experience: 1–5 Years
Qualification: B.Sc, M.Sc, B.Pharm

Key Responsibilities:

• Execute granulation, blending, compression, and capsule filling operations.
• Maintain accurate BMR documentation.
• Monitor critical process parameters.
• Ensure compliance with GMP and SOP guidelines.
• Coordinate with QA and QC for smooth batch release.

Tablet and capsule production roles demand operational efficiency, process control knowledge, and documentation discipline.

---

Engineering (QMS)

Position: Officer to Sr. Executive
Experience: 1–5 Years
Qualification: ITI, B.Tech

Key Responsibilities:

• Support engineering documentation under QMS frameworks.
• Maintain preventive and breakdown maintenance records.
• Ensure equipment qualification compliance.
• Coordinate calibration and validation activities.
• Maintain utilities and infrastructure documentation.

Engineering QMS professionals ensure that manufacturing equipment operates under validated and compliant conditions.

---

Electrician

Position: Officer to Sr. Executive
Experience: 1–5 Years
Qualification: ITI

Key Responsibilities:

• Perform preventive and breakdown maintenance of electrical systems.
• Ensure uninterrupted power supply to manufacturing units.
• Maintain electrical documentation and safety records.
• Follow plant safety protocols and SOPs.

---

CVC Operator

Position: Operator
Experience: 1–5 Years
Qualification: ITI

Key Responsibilities:

• Operate CVC labeling and packing machines.
• Monitor batch coding and labeling accuracy.
• Maintain packing documentation.
• Ensure compliance with SOP and GMP requirements.

---

Eligibility / Qualifications

Accepted Educational Background:

B.Sc (Chemistry, Microbiology, Life Sciences), M.Sc (Chemistry, Microbiology), B.Pharm, ITI (Electrical/Technical), B.Tech (Engineering).

Experience Requirement: 1–5 years in pharmaceutical manufacturing, quality assurance, quality control, production, engineering, or packing operations.

Candidates with prior exposure to GMP-regulated pharmaceutical plants will be preferred.

---

Location & Salary

Work Location: Bavla-Sanand Road, Bavla, Ahmedabad, Gujarat
Salary: Industry competitive and aligned with candidate experience and technical exposure.

Ahmedabad remains a key pharmaceutical hub, offering stable career growth across QA, QC, Production, and Engineering domains.

---

Application Process

Interested candidates may contact:
Phone: 96626 70023
Email: hrd2@stravahealthcare.com

Candidates are advised to mention the department and position clearly while applying.

---

Why Join Strava Healthcare?

• Growing pharmaceutical manufacturing organization
• Strong Quality Management Systems
• Exposure to GMP and documentation-driven operations
• Opportunities in QA, QC, Production, and Engineering
• Structured career growth in tablet and capsule manufacturing

Working in a compliance-driven pharmaceutical facility builds strong regulatory understanding and long-term industry credibility.

---

Frequently Asked Questions (FAQs)

1. What experience level is required?
1 to 5 years in pharmaceutical manufacturing or quality functions.

2. Which qualifications are accepted?
B.Sc, M.Sc, B.Pharm, ITI, B.Tech depending on department.

3. Is GMP experience mandatory?
Preferred for most technical and quality roles.

4. Which departments are hiring?
QA, QC (Reviewer & Micro), Production (Tablet/Capsule), Engineering, Electrician, CVC Operator.

5. How can I apply?
Send your CV via email or contact the provided mobile number.

---

Summary

Company	Strava Healthcare Pvt. Ltd.
Vacancies	QA Officer/Sr. Executive, QC Reviewer, QC Micro, Production (Tablet/Capsule), Engineering (QMS), Electrician, CVC Operator
Required Education	B.Sc, M.Sc, B.Pharm, ITI, B.Tech
Experience	1–5 Years

---