Regulatory Affairs Engineering Freshers Hiring in Hyderabad at Bachwell Pharma experienced pharmaceutical candidates across India.
Introduction
Bachwell Pharma has announced new career opportunities for freshers and experienced professionals in Hyderabad for Regulatory Affairs and Engineering departments. Candidates looking for Regulatory Affairs Jobs, Pharma Jobs 2026, Freshers Pharma Jobs, and M.Pharm Jobs can explore multiple openings in Drug Regulatory Affairs and Process Maintenance. The company is hiring skilled professionals for US FDA, EMA, CDSCO, and DCGI regulatory operations along with pharmaceutical engineering maintenance activities. This recruitment drive offers excellent opportunities for candidates seeking long-term growth in pharmaceutical manufacturing, compliance, validation, and regulatory submissions within the Indian pharmaceutical industry.
About Company
Bachwell Pharma is a growing pharmaceutical company engaged in manufacturing, regulatory affairs, and pharmaceutical development services. The company focuses on maintaining high-quality standards aligned with global pharmaceutical regulations including US FDA, EMA, CDSCO, and DCGI guidelines. Bachwell Pharma is known for its expertise in dossier preparation, regulatory documentation, validation support, and pharmaceutical manufacturing compliance.
The organization operates with modern pharmaceutical systems and follows industry-standard quality practices to support domestic and international regulatory markets. Its business operations include regulatory submissions, pharmaceutical engineering, packaging support, quality compliance, and lifecycle management activities. Bachwell Pharma also provides exposure to advanced pharmaceutical technologies including eCTD submissions, validation procedures, automation systems, and regulatory intelligence management. The company continues to expand its presence in the pharmaceutical sector by offering professional growth opportunities for freshers and experienced candidates across multiple functional departments.
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Job Details / Job Summary
| Particulars | Details |
|---|---|
| Company Name | Bachwell Pharma |
| Job Role | Regulatory Affairs Associate Trainee, Research Associate, Engineering Executive |
| Department | Regulatory Affairs & Engineering |
| Qualification Required | M.Pharm / M.Sc / Any Graduation |
| Experience Required | 0 – 7 Years |
| Salary Package | ₹2.5 LPA – ₹8.5 LPA (Expected) |
| Job Location | Hyderabad |
| Employment Type | Full-Time |
| Industry Type | Pharmaceutical / Healthcare |
| Shift Timing | General Shift |
| Gender Eligibility | Male & Female |
| Application Mode | Email Application |
| Selection Process | Resume Screening, Technical Interview, HR Round |
| Skills Required | eCTD, CDSCO, CMC Documentation, Validation, Maintenance |
| Official Notification Status | Verified Job |
| Application Last Date | Apply As Soon As Possible |
Available Open Positions
1. Regulatory Affairs Associate Trainee
- Department: Drug Regulatory Affairs
- Experience: Freshers
- Qualification: M.Pharm / M.Sc (Regulatory Specialization)
- Location: ALEAP, Pragathi Nagar, Hyderabad
- Vacancies: 3
2. Research Associate – Drug Regulatory Affairs
- Experience: 3–7 Years
- Qualification: M.Pharm / M.Sc (Regulatory Specialization)
- Location: ALEAP, Pragathi Nagar, Hyderabad
- Vacancies: 2
3. Executive – Engineering Process Maintenance
- Experience: 2–5 Years
- Qualification: Any Graduation
- Location: Pashamylaram IDA, Hyderabad
- Vacancies: 2
Eligibility Criteria
- Candidates must possess M.Pharm, M.Sc, or Graduation from a recognized institution.
- Freshers are eligible for Regulatory Affairs Associate Trainee positions.
- Experienced candidates with regulatory affairs exposure can apply for Research Associate roles.
- Candidates applying for engineering positions should have pharmaceutical maintenance experience.
- Applicants should possess strong communication and documentation skills.
- Knowledge of pharmaceutical compliance standards will be preferred.
- Candidates willing to work in Hyderabad are encouraged to apply.
Required Skills
- Knowledge of eCTD submission process
- Understanding of US FDA and EMA regulations
- CDSCO and DCGI documentation knowledge
- SUGAM portal handling experience
- CMC documentation preparation
- Regulatory dossier compilation skills
- Equipment validation and calibration knowledge
- IQ, OQ, and PQ validation understanding
- Pharma packaging maintenance expertise
- Strong analytical and documentation skills
- Good coordination and teamwork abilities
- Understanding of pharmaceutical compliance systems
Roles and Responsibilities
Regulatory Affairs Responsibilities
- Prepare regulatory dossiers and submission documents.
- Support eCTD Module 2 and Module 3 documentation.
- Monitor stability data according to ICH guidelines.
- Handle CDSCO and SUGAM portal submissions.
- Manage labeling and artwork compliance activities.
- Track regulatory updates related to US FDA and EMA.
- Coordinate with QA, R&D, and manufacturing teams.
- Support post-approval variations and lifecycle management.
- Prepare responses for regulatory authority queries.
Engineering Process Maintenance Responsibilities
- Perform preventive maintenance of pharmaceutical equipment.
- Troubleshoot packaging machine breakdowns.
- Support calibration and instrumentation activities.
- Maintain compliance documentation for audits.
- Coordinate with vendors for spare parts and maintenance.
- Support equipment qualification and validation activities.
- Maintain serialization and automation systems.
- Ensure smooth functioning of pharmaceutical packaging operations.
Salary Details
Bachwell Pharma offers competitive salary packages based on qualifications, technical expertise, and experience level. Freshers joining Regulatory Affairs roles may receive packages between ₹2.5 LPA and ₹4 LPA, while experienced professionals in Regulatory Affairs Jobs and Engineering positions can expect higher salary packages ranging from ₹5 LPA to ₹8.5 LPA. Additional career growth opportunities, learning exposure, and regulatory training benefits are also provided by the company.
Selection Process
The selection process at Bachwell Pharma generally includes the following stages:
- Resume Screening
HR and department teams review candidate profiles and qualifications. - Technical Assessment
Candidates are evaluated based on pharmaceutical regulatory or engineering knowledge. - Technical Interview
Shortlisted applicants attend departmental interviews focusing on job-related skills. - HR Discussion
Salary, joining timeline, and employment terms are discussed with selected candidates. - Final Selection
Selected candidates receive official communication from the company.
Why Join Bachwell Pharma?
- Exposure to global regulatory markets
- Opportunities in Regulatory Affairs Jobs and Pharma Company Hiring
- Hands-on experience with eCTD and CDSCO submissions
- Career growth for freshers and experienced candidates
- Learning opportunities in validation and compliance
- Work exposure to US FDA and EMA standards
- Professional growth in pharmaceutical engineering and maintenance
How to Apply
Interested candidates can send their updated resume to the official email addresses mentioned below:
WhatsApp Contact: +91 9014502249
Candidates should mention the applied position clearly in the email subject line and attach updated educational and experience documents before submission.
Frequently Asked Questions
1. What qualifications are required for Bachwell Pharma jobs?
Candidates with M.Pharm, M.Sc, and Graduation qualifications are eligible depending on the applied role.
2. Can freshers apply for Bachwell Pharma Regulatory Affairs Jobs?
Yes, freshers are eligible for the Regulatory Affairs Associate Trainee position.
3. What is the expected salary at Bachwell Pharma?
The expected salary ranges between ₹2.5 LPA and ₹8.5 LPA depending on experience and job role.
4. How can candidates apply for these Pharma Jobs 2026?
Applicants can apply by sending their updated CV through the official email addresses provided in the notification.