qc analyst

Star Laboratories (Pvt.) Ltd.

Education &amp; Experience:<ul><li>MSc (Chemistry) or Pharm-D (Doctor of Pharmacy) from HEC-recognized institution.</li><li>Minimum Experience 3 to 4 years</li><li>Candidates with pharmaceutical experience preferred; must not be currently enrolled in studies</li></ul>Responsibilities:<ul><li>Responsible for CTD dossier preparation, method validation and verification, and ensuring compliance with QC protocols and regulatory standards in pharmaceutical analysis.</li><li>Also responsible about CTD Dossiers and Reports</li></ul>Job Locations: Multan Road, Chung LahoreJob Type: Full-timeWork Location: In person

Sr. QC Analyst (Validation)

Lonza

<div>Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there&rsquo;s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that&rsquo;s the kind of work we want to be part of.
Join our ambitious team at Lonza AG as an Analyst IV, QC Microbiology - LSA in the beautiful state of New Hampshire, USA. This outstanding opportunity allows you to be part of a world-class manufacturing team where your skills will directly contribute to our mission of improving lives through science. As part of our ongoing growth, we're looking for dedicated individuals ready to compete on a global scale and successfully implement innovative solutions.<h2 class="jobSectionHeader">
Key responsibilities:</h2><ul><li>
Conduct and coordinate microbiological testing to ensure products meet strict quality standards</li><li>
Develop and maintain standard operating procedures (SOPs) for microbiological assays</li><li>
Analyze and interpret data, providing outstanding insights and recommendations</li><li>
Collaborate with cross-functional teams to determine root causes of microbiological issues and implement corrective actions</li><li>
Ensure compliance with regulatory requirements and internal policies</li><li>
Mentor and train junior team members, encouraging an inclusive and collaborative environment</li></ul><h2 class="jobSectionHeader">
Key requirements:</h2><ul><li>
Bachelor&rsquo;s degree or equivalent experience in Microbiology, Biology, or related field; advanced degree preferred</li><li>
Proven experience in a QC microbiology role within a manufacturing environment</li><li>
Strong knowledge of microbiological techniques and aseptic processes</li><li>
Outstanding analytical skills with the ability to strictly adhere to procedures and regulations</li><li>
Excellent communication and teamwork abilities</li><li>
Ability to manage multiple tasks and projects with flawless execution</li></ul>
This is your chance to be part of a team where your ideas can lead to significant advancements in life sciences. We can't wait to see the outstanding contributions you'll make!
Every day, Lonza&rsquo;s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.</div>

QC Analyst IV Microbiology - LSA

<div>Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there&rsquo;s no magic formula for how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that&rsquo;s the kind of work we want you to be part of!
The QC Analyst I - Raw Materials is responsible for performing routine and specialized analytical/compendial testing of incoming raw materials in compliance with Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs). Working within a collaborative team, you'll be essential in ensuring the quality and timely release of materials to meet the needs of internal manufacturing and external customers. This role requires the ability to apply job skills to semi-routine assignments and recognize deviations from accepted practice. Find out more about what a role at Lonza in Portsmouth, NH could look like for you, by watching this short video.
Schedule: Sunday - Wednesday, 8:00 AM - 6:30 PM
What will you get?<ul><li>
An agile career and dynamic working culture</li><li>
An inclusive and ethical workplace</li><li>
Compensation programs that recognize high performance</li><li>
Comprehensive benefits including Medical, Dental, Vision, PTO, and more</li></ul>
The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.
What you&rsquo;ll do:
<ul><li>Raw Material Testing: Perform routine and specialized raw material testing, including IR/Raman spectroscopy and wet chemistry analysis, strictly according to Standard Operating Procedures and Pharmacopeia methods.</li><li>
Data Management &amp; Analysis: Accurately record, analyze, and review all data related to testing. Apply Data Integrity (DI) principles in all aspects of work, in compliance with company policies, guidelines, and procedures.</li><li>
Compliance &amp; Problem Solving: Work on assignments where the ability to recognize deviations from accepted practice is required. Address problems of moderate scope in which analysis of the situation or data requires a review of identifiable factors.</li><li>
Laboratory Support: Perform general lab support activities, including housekeeping, equipment maintenance, and inventory/ordering of supplies. Maintain compliance with all required training.</li><li>
Project Execution: Perform project-related tasks as assigned with general instructions, contributing to departmental and site goals.</li></ul>
What we&rsquo;re looking for:<ul><li>
Education: A High School Diploma or equivalent is required. An Associate's Degree in Microbiology, Biochemistry, or a related science field is preferred.</li><li>
Experience: Proven ability to apply job skills and company policies/procedures to complete a variety of tasks, preferably in a regulated environment.</li><li>
Schedule &amp; Compliance: Must be available to work the Sunday - Wednesday, 8:00 AM - 6:30 PM schedule. A foundational understanding of cGMP is necessary.</li></ul>
Every day, Lonza&rsquo;s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference!
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.</div>

QC Analyst I - Raw Materials (First Shift)

Regal Laboratories

B-PHARMA, M-PHARMA/ B.SC, M.SC (MINIMUM EXPERIENCE-2-5 YEARS)Job Type: Full-timePay: &#8377;20,000.00 - &#8377;25,000.00 per monthWork Location: In person

QC Analyst (FG) (HPLC AGILENT)

HRSG

1. To ensure the all the batch packets are error free, complete and reviewed on time.2. To ensure the all the batch packets are released on time in company, and Customer&rsquo;s SAP system in accordancewith release tracker and batch release time. Zero% delay is expected.3. To ensure the all Raw &amp; Pack materials are released in the company SAP with all the recording of Elogand by complying with technical standard (IRMS/IPMS) and, minimum requirements of COA.4. To ensure customer&rsquo;s online FP release tracker is being effectively updated on time.5. Calibrate the daily calibrations of the equipment&rsquo;s as per the requirements and internal calibration plan.6. Incident reporting on time and implements all the Site safety systems in Lab.7. To ensure quality Q-BOS is being effectively performed by analyst on daily basis and related issues are beingreported and resolved timely.8. In case of any A shift analyst on leave and absent, will flow to work and do the RM/PM/FP Analyst role.9. On time completion of special assigned task depending upon the urgency and severity of the task withoutaffecting rest of the routine tasks.10. To ensure the 5Sing in Lab Office. And Lab should be clean at the time of shift handover takeover.11. To ensure the Monthly batch packets records in bundles. Single, Blank and Bundle separately.12. 100% mandatory Quality trainings completion13. Ensure zero critical observations in Audit due to any quality outages14. 100% Participation in Q-BOS and Quality Alerts to be ensured15. &ge; 98% team training completion on Quality Mandatory &amp; operational SOPs to be ensured.16. Zero repeated QIs, repeated customer/consumer complaints and SQIs/CQIs to be ensured.17. 100% On-Time CAPA closure and On-Time Investigation Completion18. 100% on-time QA action completion (through provision of adequate resources)19. 100% on time self QA training/refresher completion.Company Location: HUB BalochistanJob Types: Full-time, Contract Contract length: 12 monthsPay: Rs70,000.00 - Rs80,000.00 per monthApplication Question(s):<ul><li>Do you have experience QA / QC in FMCG company?</li></ul>Can you operate company SAP system? Can you commute from Karachi to Hub?Education:<ul><li>Intermediate (Required)</li></ul>Experience:<ul><li>QA/ QC FMCG: 2 years (Required)</li></ul>Work Location: In person

QA / QC

Acino Pharma

Acino is a Swiss pharmaceutical company, leader in advanced drug delivery technologies. We have a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America, and we operate in some of the most dynamic countries of the world. We value courage, commitment, trust, and empathy and provide an environment that supports initiative and effort. We are proud to be action-oriented and open-minded, with a strong focus on quality and product availability, even in remote and hard-to-reach areas of the world.
We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our Quality team in Dubai, UAE Site- Acino Pharmaceuticals FZ LLC
 
Quality Control Analyst will be responsible for performing analytical testing, maintaining laboratory resources, ensuring compliance with quality and safety standards, and supporting product release, method transfers, and validations. He /She will work with advanced analytical instruments, uphold data integrity principles, and ensure full compliance with GMP requirements to maintain product quality, safety, and efficacy.
 
Job Responsibilities
<ul>
<li>Perform analysis of raw materials, packaging materials, bulk products, finished products, in-process samples, stability samples, process/cleaning validation samples, and miscellaneous samples as per approved methods and protocols.</li>
<li>Ensure all activities comply with GLP, GMP, and ALCOA++ principles.</li>
<li>Operate major analytical instruments including HPLC, GC, Dissolution Apparatus, UV-Vis Spectrophotometer, and IR.</li>
<li>Perform daily verification, calibration, and routine maintenance of instruments as per SOPs.</li>
<li>Maintain an up-to-date inventory of reference standards, working standards, impurity standards, analytical columns, reagents, chemicals, and consumables.</li>
<li>Conduct qualification of working standards against reference or primary standards.</li>
<li>Prepare volumetric solutions and standardize them for routine use.</li>
<li>Prepare, review, and update SOPs, test methods, and specifications as needed.</li>
<li>Record all data accurately, clearly, and in real-time following GLP requirements.</li>
<li>Report and support investigations for any OOS, OOT, incidents, or non-compliance activities.</li>
<li>Initiate and support Change Control, CAPA, and Deviation processes as required.</li>
<li>Follow safety procedures and use the recommended PPE for all QC activities.</li>
<li>Ensure compliance with EHS policies and safe work practices in the laboratory.</li>
<li>Support analytical validation/verification and cleaning validation studies.</li>
<li>Participate in laboratory improvement initiatives.</li>
<li>Carry out additional tasks assigned by the QC Manager in line with department objectives.</li>
</ul>
 
Qualifications &amp; Skills:
<ul>
<li>Bachelor s degree in chemistry, pharmaceutical sciences, or related discipline.</li>
<li>1 3 years of experience in a pharmaceutical QC laboratory.</li>
<li>Hands-on experience with HPLC, GC, Dissolution, UV, and IR instruments.</li>
<li>Knowledge of LIMS and SAP systems is preferred.</li>
<li>Good understanding of GMP, GLP, and data integrity principles (ALCOA++).</li>
<li>Strong attention to detail, analytical thinking, and problem-solving skills.</li>
<li>Effective communication and teamwork abilities.</li>
</ul>
 
This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!
 
Please apply via our HR system here.

Quality Control Analyst

Amros Pharmaceuticals

Hirings.1- Senior QC Officer1-2 years of experience Male &amp; Female both can apply2- QC Executive 4-5 years of Experience Only Males RequiredNote:Must Have Pharmaceutical ExperienceQC ExecutiveWe are looking for a sharp, experienced QC Executive to join our Quality Control team.Core Responsibilities:Execute and oversee analytical testing of raw materials, in-process samples, and finished products.Ensure strict adherence to all regulatory guidelines.Review and approve QC records, analytical reports, and maintain laboratory documentation.Investigate OOS/OOT results and manage deviations/CAPA.Participate in analytical method validation, transfer, and equipment qualification.Qualifications:Bachelor's or Master's degree in Pharmacy or a related science field.4-5 years of mandatory QC experience in Pharma Manufacturing.Strong technical proficiency in major analytical techniques and regulatory compliance (cGMP).Excellent communication, documentation, and problem-solving skills.If you are detail-oriented and committed to pharmaceutical quality, apply today to help us ensure product safety and efficacy!Apply Here: hr.recruitment@amrospharma.comJob Type: Full-timeExperience:<ul><li>Pharmaceutical: 2 years (Required)</li></ul>Work Location: In person

Quality Control Executive

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