Senior QC Analyst-Pharma

Job Description

Horizon Biolabs Pvt Ltd. is a GLP compliant Pharmaceutical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries .

We are looking for :

Candidate with Msc/Bsc/Bpharm/Mpharm having minimum 03-05 years of experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry as a Sr.QC Analyst.

About the job

The Quality Control Analyst will report to the Manager of Quality. The Quality Control Analyst will stay current regulatory systems and other pertinent regulating bodies to ensure the Quality Control Laboratories and associated activities throughout the facility are compliant and continuously improved upon. The Quality Control Analyst will ensure the analytical/microbiology laboratories are in compliance with current regulatory practices.

Essential Duties And Responsibilities

• Responsible for managing the QC laboratory in accordance with cGMP.
• organize and maintain all departments and laboratory processes, procedures and administrative duties.
• Assure that all customer samples are tested in accordance with all regulatory, and customer requirements, as applicable.
• Provide guidance to team members to resolve problems with instruments, test methods, lab chemicals, standards, and samples.
• approvals, rejections, documentation status, and any other QC matters .
• Assure adequate communication of priorities exists between the lab and other departments and within the lab.
• Investigate deviations and write exception documents as required, utilizing problem solving tools as needed.
• Responsible for investigating and processing Deviations, Out of Specifications, and Out of Trend, QC events. Identify and report non-conformances/deviations/out-of-specification events.
• Manages process optimization program that includes continual improvement programs for analyses, human capital development and management systems
• Facilitate the evaluation of new testing applications and instrumentation. Assist in the purchase and commission of analytical and microbiology instrumentation. Ensure there are efficient instruments for the workload of samples.
• Prepare justification for new lab equipment. Prepare purchase orders and coordinate authorization and procurement. Arrange installation and qualification.

Experience

• 3+ years of QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.
• Must have hands on experience and should be able to guide juniors on all the laboratory instruments (HPLC/GC/PSD/IR/TOC/POTENTIOMETRY/DSC/TGA etc..)
• Method Development/validation experience required.
• Protocol preparation/Report preparation experience is a must.
• Experience implementing and maintaining departmental metrics
• Prior experience working with external testing laboratories

Education

• Bachelor’s /Masters degree in Science related field required.

Skills and Knowledge:

• Demonstrated leadership and organization skills
• Excellent oral and technical writing skills with the ability to interface effectively and professionally at all levels

Abilities

• Ability to develop and lead a high performing team.
• Communicate clear work plans, coordinate staff schedules, training and standardize work hours among the staff when possible.
• Work with various staff members to evaluate and improve processes, through informal and formal channels.
• Ability to work on cross functional teams and apply influencing skills in a matrix environment
• Must be able to develop solutions for simple and complex problems, which require a high degree of ingenuity, creativity and innovation. Challenges are frequently unique and solutions may serve as precedent for future decisions, which effect the entire organization.

Job Type: Full-time

Schedule:

• Day shift

Education:

• Msc/M Phrama/B Pharma/Bsc(Chemistry)

Experience:

• total work: 03-05 years (Required)
• Immediate Joiner
• Candidates from Hyderabad only.
• Candidates from QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.

Job Type: Full-time

Benefits:

• Provident Fund

Application Question(s):

• QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.Are you from Hyderabad?Willing to Join immediately(07-10 days),candidates related to other fields applications will not considered.
• are you from Hyderabad?

Location:

• Hyderabad, Telangana (Preferred)

Work Location: In person

Job Type: Full-time

Pay: ₹25,000.00 - ₹35,000.00 per month

Benefits:

• Provident Fund

Application Question(s):

• Are you currently staying in Hyderabad?
• Are you having QC lab experience in CRO/pharmaceutical industry in a cGMP environment?
• are you ready to join immediately?(within 7 days)

Work Location: In person