ACME Generics Pvt. Ltd -Openings for Packing / Quality Assurance Departments

ACME Generics Pvt. Ltd -Openings for Packing / Quality Assurance Departments

Are you passionate about contributing to the global healthcare industry? ACME Generics Pvt. Ltd., a USFDA approved facility with over three decades of expertise in contract manufacturing, invites dynamic individuals to join our team in Baddi, Himachal Pradesh.

Department: Packing (OSD)

Section: Primary

Position: Officer/Sr. Officer

Experience: 1-5 years

Qualifications: B.Pharm

In this role, you will play a pivotal part in the primary packing section, ensuring the highest standards of quality in the production of oral solid dosage forms. If you have 1-5 years of experience and hold a B.Pharm qualification, we encourage you to apply.

Department: QA

Section: APQR

Position: Officer/Sr. Officer

Experience: 1-5 years

Qualifications: B.Pharm

As part of our Quality Assurance team, specifically in the APQR section, you will be responsible for maintaining meticulous standards in our processes. If you have 1-5 years of experience and a B.Pharm qualification, this position might be the next step in your career journey.

Location: Baddi, Himachal Pradesh

If you are enthusiastic about making a difference in the healthcare industry and thrive in a dynamic environment, we want to hear from you! Interested candidates can share their resumes via WhatsApp at 8219249371 or through email at hr@acmegenerics.in.

Job Category: pharma
Job Type: Full Time
Job Location: Baddi (H.P

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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