Sekhmet Walk-in Production – Production ,Quality Control

BSc MPharm Vacancies at Sekhmet Hyderabad

BSc, MSc, BPharm, MPharm vacancies (0–5 yrs) at Sekhmet Pharmaventures, Hyderabad. Walk-in on 28 Feb 2026.

Sekhmet Pharmaventures, part of the Optimus group, is conducting a walk-in interview drive for Production and Quality Control professionals in Hyderabad. This recruitment initiative is aimed at candidates with 0 to 5 years of experience who want to build or accelerate their careers in bulk drugs and pharmaceutical manufacturing. If you are looking to enter or grow within API manufacturing, quality control laboratory operations, or regulated pharma production environments, this walk-in drive offers a structured and credible platform.

The company is hiring for its manufacturing facilities at Dothigudem (Unit 1) and Ramalingampally (Unit 3). Candidates seeking pharmaceutical jobs in Hyderabad, API manufacturing careers, GMP production roles, and QC analyst opportunities should carefully review the details below and attend the interview with complete documentation.

Company Overview

Sekhmet Pharmaventures operates under the Optimus group, a recognized name in the bulk drugs and active pharmaceutical ingredients (API) manufacturing sector. The organization is involved in the development and large-scale production of pharmaceutical intermediates and APIs that support global healthcare supply chains.

The company serves regulated and semi-regulated markets and follows current Good Manufacturing Practices (cGMP) to ensure quality, safety, and regulatory compliance. With growing demand in the API export market, pharmaceutical manufacturing companies like Sekhmet play a critical role in delivering affordable and high-quality medicines worldwide.

Key strengths of Sekhmet Pharmaventures include:

• Bulk drug manufacturing expertise
• Regulatory-compliant production systems
• Advanced quality control laboratory infrastructure
• Skilled R&D and technical teams
• Consistent expansion across API manufacturing units

Professionals joining Sekhmet gain exposure to real-time pharmaceutical production cycles, quality assurance protocols, stability testing procedures, and regulatory documentation systems. This experience strengthens long-term career prospects in pharmaceutical production, regulatory affairs, and quality assurance domains.

Job Role & Responsibilities

Sekhmet Pharmaventures is hiring for the following departments:

Production – API / Bulk Drug Manufacturing

Qualification Required: B.Sc, M.Sc, B.Tech, Diploma
Experience: 0–5 Years

Production professionals will be responsible for executing manufacturing operations in compliance with SOPs and cGMP guidelines.

Key Responsibilities:

• Handling bulk drug production processes
• Monitoring chemical reactions and batch processes
• Equipment operation and process parameter control
• Maintaining batch manufacturing records (BMR)
• Coordinating with Quality Control for in-process sampling
• Ensuring safety and environmental compliance
• Supporting scale-up and validation activities

Candidates with exposure to API manufacturing, chemical process plants, or pharmaceutical production units will have an advantage. Freshers with strong academic understanding of pharmaceutical manufacturing technology may also apply.

This role directly contributes to large-scale API production, making it a high-demand pharmaceutical manufacturing career option.

Quality Control – Analytical Laboratory

Qualification Required: M.Sc, B.Pharm, M.Pharm
Experience: 0–5 Years

Quality Control professionals will support analytical testing of raw materials, intermediates, and finished API products.

Key Responsibilities:

• Performing analytical testing using instruments such as HPLC and GC
• Conducting wet analysis and chemical testing
• Handling stability studies and method validation
• Preparing analytical reports and documentation
• Following GLP and data integrity practices
• Supporting regulatory audit documentation

Candidates should possess a clear understanding of pharmaceutical quality control standards, analytical chemistry principles, and laboratory compliance requirements.

QC roles are considered high-value pharmaceutical careers due to increasing regulatory scrutiny and global compliance requirements.

Eligibility / Qualifications

Candidates must meet the educational criteria relevant to the department they are applying for.

Eligible Courses (comma-separated as applicable):

B.Sc Chemistry, B.Sc Industrial Chemistry, B.Sc Life Sciences, M.Sc Chemistry, M.Sc Analytical Chemistry, M.Sc Organic Chemistry, M.Sc Pharmaceutical Chemistry, B.Tech Chemical Engineering, Diploma in Chemical Engineering, Diploma in Pharmacy, B.Pharm, M.Pharm

Experience Requirement:

• 0 to 5 years of relevant pharmaceutical or chemical industry experience
• Freshers with strong academic knowledge may apply
• Understanding of GMP compliance and documentation preferred

Skill Expectations:

• Strong technical fundamentals
• Awareness of pharmaceutical regulatory standards
• Basic knowledge of cGMP and GLP
• Documentation accuracy and discipline

Location & Facilities

Plant Locations:
Dothigudem (Unit 1)
Ramalingampally (Unit 3)

For Unit 3 (Ramalingampally), the company provides bus transportation from Ameerpet. Free canteen facilities are also available for employees. These benefits reduce commuting burden and improve employee convenience.

While specific salary details are not disclosed, compensation will be aligned with experience, technical skills, and industry standards in the Hyderabad pharmaceutical sector.

Hyderabad remains one of India’s leading pharmaceutical manufacturing hubs, especially for bulk drugs and API exports. Working in this ecosystem strengthens professional credibility in chemical manufacturing, regulatory compliance, and large-scale pharmaceutical operations.

Walk-In Interview Details

Interview Date: 28th February 2026
Timings: 8:00 AM to 3:00 PM

Venue:
Jubilee Park
2-3-229/1, Uppal
LB Nagar – Uppal Road
Nagole, Hyderabad

Candidates should report within the mentioned time window to ensure smooth interview coordination.

Documents to Carry

Applicants attending the walk-in interview must carry:

• Updated Resume
• Educational certificates (original and copies)
• Experience letters (if applicable)
• Recent passport-size photographs
• Government ID proof

Incomplete documentation may delay evaluation or disqualify participation.

Why Consider Sekhmet Pharmaventures?

Pharmaceutical manufacturing and API production are among the most stable and high-growth segments within the life sciences industry. Companies engaged in bulk drug manufacturing face strict international regulatory standards, making hands-on experience highly valuable.

Working in Production builds expertise in:

• Chemical process optimization
• GMP documentation
• Industrial safety systems
• Validation and scale-up activities

Working in Quality Control builds expertise in:

• Analytical instrumentation (HPLC, GC)
• Regulatory audit readiness
• Pharmaceutical compliance
• Method development and validation

These competencies significantly improve long-term earning potential in pharmaceutical quality assurance, regulatory affairs, and technical operations.

Career Growth Opportunities

Candidates starting in entry-level Production or QC roles often progress into:

• Senior Production Officer
• QC Analyst / Senior QC Executive
• QA Officer
• Validation Specialist
• Regulatory Affairs Associate
• Plant Operations Supervisor

The pharmaceutical industry rewards technical competence, regulatory awareness, and documentation accuracy. Early exposure to API manufacturing systems accelerates career growth compared to non-regulated chemical industries.

Frequently Asked Questions (FAQs)

1. Are freshers eligible for this walk-in?

Yes. Candidates with 0–5 years of experience can apply. Freshers with relevant degrees are eligible.

2. Is prior API experience mandatory?

It is preferred but not mandatory for freshers. Basic understanding of pharmaceutical manufacturing processes is important.

3. What departments are hiring?

Production and Quality Control departments are hiring.

4. Is transportation provided?

Yes. Bus facility is available from Ameerpet to Ramalingampally (Unit 3).

5. What is the salary range?

Salary depends on experience and technical skills. It will be discussed during the HR round.

6. Is this role suitable for long-term pharma careers?

Yes. Experience in API manufacturing and QC analytics significantly strengthens future career prospects in regulated pharmaceutical markets.

---

Walk-In Drive Summary

Company	Sekhmet Pharmaventures (Optimus Group)
Vacancies	Production – Production Executive / Production Officer; Quality Control – QC Analyst / QC Executive
Required Education	B.Sc, M.Sc, B.Tech, Diploma, B.Pharm, M.Pharm
Experience	0–5 Years