Sanzyme Hiring Production QA QC

BPharm MSc Production QA QC Jobs Telangana

BPharm/MPharm/MSc/BTech vacancies (0–10 yrs) at Sanzyme Pvt Ltd Injectable Unit, Shamirpet Telangana. Apply now.

Sanzyme Pvt Ltd is hiring for multiple positions at its formulation injectable manufacturing unit located at Kolthur Village, Shamirpet, Telangana. The company is inviting applications from qualified and experienced professionals in Drug Product (DP) Production, Drug Substance (DS) Production, Quality Assurance (QA), and Quality Control (QC – Microbiology).

If you are looking for injectable manufacturing jobs in Telangana, pharmaceutical production careers, microbiology QC roles, or QA executive opportunities in a GMP-regulated formulation plant, this is a strong opportunity to work in a specialized injectable unit. Immediate joiners are preferred.

Company Overview

Sanzyme Pvt Ltd operates a pharmaceutical formulation facility focused on injectable products. Injectable manufacturing is one of the most regulated and technically demanding segments within the pharmaceutical industry. Facilities producing sterile dosage forms must comply with stringent cGMP standards, aseptic processing protocols, environmental monitoring systems, and regulatory documentation requirements.

Working in an injectable unit provides exposure to:

• Sterile manufacturing and aseptic processing
• Regulatory-compliant documentation systems
• Quality Management Systems (QMS)
• Training Management Systems (TMS) and Document Management Systems (DMS)
• Microbiological contamination control practices

Injectable manufacturing plants are regularly inspected by national and international regulatory authorities. Professionals with sterile manufacturing experience are consistently in high demand across the pharmaceutical sector.

Job Role & Responsibilities

Sanzyme Pvt Ltd is hiring across the following departments:

1. DP Production – Trainee Executive / Executive

Qualification: M.Sc, B.Pharm, M.Pharm
Experience: 0–5 Years
Preference: Male Candidates
Industry Exposure: Injectable Manufacturing Unit

Key Responsibilities:

• Executing drug product (DP) manufacturing activities in sterile areas
• Operating filling, compounding, and formulation equipment
• Ensuring adherence to batch manufacturing records (BMR)
• Maintaining cGMP compliance in production areas
• Supporting aseptic process validation activities
• Coordinating with QA and QC teams for in-process checks

Candidates must demonstrate understanding of sterile production operations and regulatory compliance within injectable units.

2. DS Production – Executive / Senior Executive

Qualification: B.Tech Biotechnology, M.Tech Biotechnology
Experience: 5–10 Years
Preference: Male Candidates
Expertise: Downstream Processing

Key Responsibilities:

• Managing downstream processing operations in biologics or related production streams
• Handling purification, filtration, and process optimization steps
• Monitoring critical process parameters
• Maintaining batch production documentation
• Ensuring adherence to regulatory and cGMP guidelines

Strong experience in downstream processing within pharmaceutical or biotechnology manufacturing is required.

3. Quality Assurance – Executive

Qualification: B.Pharm, M.Pharm
Experience: 0–5 Years
Gender: Male/Female
Special Requirement: Knowledge of TMS & DMS in Injectable Unit

Key Responsibilities:

• Handling training activities within QA department
• Managing Training Management System (TMS)
• Maintaining Document Management System (DMS)
• Ensuring SOP compliance and documentation accuracy
• Supporting audit preparation and compliance verification
• Monitoring quality systems in sterile production areas

QA professionals play a central role in regulatory compliance, documentation review, and maintaining inspection readiness.

4. Quality Control – Microbiology (Trainee Executive / Executive)

Qualification: B.Sc Microbiology, M.Sc Microbiology
Experience: 0–5 Years
Preference: Male Candidates
Industry Exposure: Injectable Unit

Key Responsibilities:

• Performing microbiological testing for sterile injectable products
• Conducting environmental monitoring in classified areas
• Supporting sterility testing and microbial limit testing
• Maintaining microbiology laboratory records
• Ensuring compliance with data integrity and ALCOA principles

Microbiology QC professionals in injectable plants are responsible for sterility assurance and contamination control, which are critical for patient safety.

Eligibility / Qualifications

Educational Qualifications (comma-separated):

B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Microbiology, B.Sc Microbiology, B.Tech Biotechnology, M.Tech Biotechnology

Experience Requirements:

• 0–5 years for DP Production, QA, and QC Microbiology roles
• 5–10 years for DS Production (Downstream Processing)
• Prior experience in injectable or sterile manufacturing preferred

Core Competencies:

• Knowledge of cGMP guidelines
• Understanding of sterile manufacturing protocols
• Documentation discipline and audit readiness
• Familiarity with QMS, TMS, and DMS systems (for QA role)

Candidates without injectable manufacturing exposure may face limitations in role suitability.

Location & Work Details

Work Location: Sanzyme Pvt Ltd, Kolthur Village, Shamirpet, Telangana

Shamirpet is emerging as a pharmaceutical and biotechnology cluster near Hyderabad. Working in this region provides strong exposure to regulated pharmaceutical manufacturing operations.

Salary will be determined based on:

• Experience in sterile manufacturing
• Technical expertise in production or microbiology
• Downstream processing exposure (for DS role)
• Current CTC and notice period

Injectable manufacturing and biologics production roles are considered high-value pharmaceutical career paths due to regulatory complexity and technical specialization.

Application Process

Immediate joiners are preferred.

Interested candidates can apply through:

• WhatsApp: 7032837394
• Email: ramakrishna.reddy@sanzyme.com

Application Steps:

1. Update your resume highlighting injectable or sterile plant experience.
2. Mention specific exposure to downstream processing (for DS role).
3. Include experience in TMS/DMS systems (for QA role).
4. Share your resume via WhatsApp or email.

Shortlisted candidates will be contacted for further discussion.

Why Injectable Manufacturing Careers Offer Strong Growth

Injectable dosage forms require strict sterility, validated cleanroom environments, and regulatory oversight. Professionals with experience in sterile production, microbiological testing, and quality assurance systems are highly valued across the pharmaceutical industry.

Working in injectable units strengthens expertise in:

• Aseptic process control
• Regulatory compliance documentation
• Environmental monitoring systems
• Quality management frameworks
• Downstream processing in biotechnology

These competencies significantly enhance long-term career stability and salary growth.

Career Growth Opportunities

Professionals joining Sanzyme may progress toward:

• Production Manager – Injectable Unit
• QA Compliance Manager
• Microbiology Lab Head
• Bioprocess / Downstream Processing Manager
• Sterile Manufacturing Specialist

Experience in injectable and biologics production environments is highly transferable across global pharmaceutical companies.

Frequently Asked Questions (FAQs)

1. Are freshers eligible?

Yes, for DP Production, QA, and QC Microbiology roles (0–5 years).

2. Is downstream processing experience mandatory for DS role?

Yes, 5–10 years of relevant downstream experience is required.

3. Is injectable manufacturing exposure important?

Yes, especially for Production and QC Microbiology roles.

4. How can I apply?

Send your resume via WhatsApp to 7032837394 or email ramakrishna.reddy@sanzyme.com.

5. Are immediate joiners preferred?

Yes, immediate joiners will be given preference.

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Job Summary

Company	Sanzyme Pvt Ltd
Vacancies	DP Production – Trainee Executive/Executive; DS Production – Executive/Sr Executive; QA Executive; QC Microbiology – Trainee Executive/Executive
Required Education	B.Pharm, M.Pharm, B.Sc/M.Sc Microbiology, B.Tech/M.Tech Biotechnology
Experience	0–5 Years (DP/QA/QC); 5–10 Years (DS Production)