5– 5 years

• Conduct/plan analytical, pre formulation and stability studies
• Cosmetic Formulation Development using herbal extracts and non herbal actives.
• Work closely with Product Testing & Evaluation and Scale Up during development.
• Participate in cross functional teams, and internal collaboration with Production, Purchase, QC and biochemistry department.
• Write/review protocols, reports, test methods and batch records.
• Review QC documentation, data, reports from analytical, formulation and clinical packaging CRO’s.
• Vendor development with regular presentations to the marketing team and vendors on new concepts.
  

4- 8 Yrs

• An ideal candidate should be well versed in International regulatory aspects. Hands on experience in product registrations in South East Asia, GCC, Europe, Africa, Latin America, Andean & Carrebean countries. The candidate should have experience in handling regulatory documentation for submission to TGA, MCC, MHRA and USFDA. Should have experience in preparing CTD.

4– 5 years

• Experience in preparing and delivering scientific presentations is desirable. Proficiency in scientific/medical writing, literature/patent searches would be an added advantage.

8 – 10 years

• Lead a team of scientists
• Good leadership and communication skills
• Knowledge of regulatory requirements
• Assist in analytical development
• Experience in novel drug delivery systems
• Product Costing
• Production scale up and technology transfer.

2 – 5 years

• Development of solid and semi solid dosage forms
• Handle sustained release and modified release dosage forms
• Manage lab scale equipment for solid dosage form manufacture
• Literature collection and pre-formulation studies
• Stability testing protocols

2 – 5 years

• Development of creams & solutions
• Knowledge of Herbal extract
• Literary collection & pre formulation studies
• Stability testing protocols
• Ability to handle lab scale equipment
  

M. Sc / M. Pharm / Ph.D

3 – 5 yrs

• Analysis of biological samples for the estimation of drugs and experience in handling latest equipments like LCMS, HPLC, HPTLC, GC
• Estimation of Bio availability/ Bio equivalence development and validation of analytical methods.
• Develop and implement new LC/MS or other methodologies for profiling metabolites in different matrices.
• Qualify, validate, and transfer analytical methods; write SOPs.

Minimum 7 yrs

• Knowledge of protecting groups involved in Peptide Synthesis, first-hand expertise in solid/ solution phase synthesis including scale-up competence. Experience in therapeutic peptides, preferably cyclic peptides and structural characterization.

Ph.D

2 years and above

• Operating/maintaining an LC/MS equipment with skills in reliable data generation and interpretation; especially a professional who has the potential to identify trace impurities in APIs with profound skills in normal HPLC operation.

2 years and above

• Experience of having worked on a modern GC/MS system with demonstrated ability to identify components using mass spectral fragmentations. Knowledge and use of diverse columns in GC separation methods is essential. Experience in spatial and new derivatization techniques for insoluble substances is a requisite.

Fresh/ Experienced

• Proficiency in multistep synthesis; good knowledge of mechanistic and synthetic chemistry with a flair for purification techniques and strong spectroscopic interpretation skills. 

Ph.D

Fresh/ experienced

• Strong background in isolating compounds from plant materials and skill in separation techniques. Flair in pharmacology to identify targets and developing new plant source for actives.

5 to 10 years industrial experience in scale up Chromatography.

Ph.D. / M.Sc. / M.Pharm

3-5 years

M.Sc. Organic Chemistry / M.Pharm / Ph.D

Fresh / 2 years.

Graduate

8- 10 Yrs

1-2 years

• Promotion of healthcare products to doctors and medical institutions.

MBA.

Fresh / Above 2 years experience.

Diploma in Chemical Engineering.

Fresh / Above 2 years experience.