Tue, April 13, 2021

Company Overview

Solid State Pharma Inc. (SSPI) is a leader in the delivery of crystallization engineering services including screening and selection of polymorphs, co-crystals, salts, and crystallization process development and optimization. SPPI has experienced great success with the workflows that have been developed by combining fundamentals of crystallization and solid form science with years of experience and high throughput techniques. SSPI is conducting research on pharmaceutical crystallization engineering, polymorph screening, salt screening, co-crystal screening, chiral resolution, polymorph quantification, converting amorphous material to crystalline solid, chemical and crystallization process modeling. SSPI is working with a large number of pharmaceutical companies across the globe to help them fully understand the solid state and crystallization of their drug candidates.

About Halifax, Nova Scotia

Halifax is one of the most beautiful and historic Canadian cities. Located on the coast of the Atlantic Ocean, there are numerous parks, campsites, trails and rivers around the city for outdoor activities. City life is also superb. With a population of more than 400,000, Halifax is home to many cultural attractions, museums, art galleries, pubs and clubs. The city hosts three major universities and many community colleges. The beautiful Annapolis valley, which is home to the highest tides in the world, and also mountainous Cape Breton, are within a few hours drive from Halifax. Halifax has one of the mildest winters in Canada as well as one of the most pleasant summers, which you can enjoy on the beautiful water front boardwalk.


The “Reviewer” position is a key contributor to the ongoing research communication activities at SSPI reporting to the Quality and Administration Manager. “Reviewer” will contribute through supporting company operations by proof-reading and reviewing the weekly and final reports prepared by the technical team. The “Reviewer” will be interacting with a highly technical team in the fast pace pharmaceutical industry.

Job Responsibility

Review documents and reports for grammar, spelling, formatting and style

Ensure the content meets the templates and requirements outlined by company policies

Make corrections and suggest edits to the document

Practice and maintain confidentiality to the highest standards

Other responsibilities as assigned

Education & Experience

A minimum of BSc or BA degree. A science background, chemistry, biology, pharmaceutical sciences, biochemistry, molecular biology or related is preferred. Strong writing skills/experience is required.


Excellent attention to detail with strong grammar and punctuation are a must

Ability to use Microsoft office software is a must

Good communication skills are required

Ability to work within tight deadlines in a fast pace environment is required

Technical writing proficiency is an asset

Strong organizational skills are an asset

Ability to work well in a collaborative environment or independently        

Closing Date

Open until filled.

Contact information

Please submit resume and cover letter to Three references are needed for candidates who are shortlisted.

Ready to collaborate? Let’s work together